Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51411 |
| ensemblid | ENSG00000110934.13 |
| hgncid | 1053 |
| symbol | BIN2 |
| name | bridging integrator 2 |
| refseq_nuc | NM_016293.4 |
| refseq_prot | NP_057377.4 |
| ensembl_nuc | ENST00000615107.6 |
| ensembl_prot | ENSP00000483983.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 51281038 |
| end | 51324174 |
| strand | - |
| ver | v1.2 |
| region | chr12:51281038-51324174 |
| region5000 | chr12:51276038-51329174 |
| regionname0 | BIN2_chr12_51281038_51324174 |
| regionname5000 | BIN2_chr12_51276038_51329174 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 565 | 285 | 50 | 60 | 128 | 10 | 36 | 95 | BIN2_chr12_51276038_51329174 | BIN2 | MAEGK others(560): Show |
chr12 | 51276038 | 51329174 |
| a0002 | 0/0 | 565 | 40 | 7 | 3 | 30 | 0 | 0 | 25 | BIN2_chr12_51276038_51329174 | BIN2 | MAEGK others(560): Show |
chr12 | 51276038 | 51329174 |
| a0003 | 1/0 | 565 | 32 | 26 | 1 | 0 | 0 | 4 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | MAEGK others(560): Show |
chr12 | 51276038 | 51329174 |
| a0004 | 0/0 | 565 | 31 | 8 | 3 | 16 | 2 | 2 | 12 | BIN2_chr12_51276038_51329174 | BIN2 | MAEGK others(560): Show |
chr12 | 51276038 | 51329174 |
| a0005 | 0/0 | 565 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | MAEGK others(560): Show |
chr12 | 51276038 | 51329174 |
| a0006 | 0/0 | 565 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | MAEGK others(560): Show |
chr12 | 51276038 | 51329174 |
| a0007 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | MAEGK others(560): Show |
chr12 | 51276038 | 51329174 |
| a0008 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | MAEGK others(560): Show |
chr12 | 51276038 | 51329174 |
| a0009 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | MAEGK others(560): Show |
chr12 | 51276038 | 51329174 |
| a0010 | 0/0 | 43 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | MAEGK others(38): Show |
chr12 | 51276038 | 51329174 |
| a0011 | 0/0 | 565 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | MAEGK others(560): Show |
chr12 | 51276038 | 51329174 |
| a0012 | 0/0 | 565 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | MAEGK others(560): Show |
chr12 | 51276038 | 51329174 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1695 | 250 | 46 | 56 | 104 | 10 | 33 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0001c0004 | 0/0 | 1695 | 30 | 3 | 4 | 20 | 0 | 3 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0001c0009 | 0/0 | 1695 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0001c0019 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0002c0002 | 0/0 | 1695 | 34 | 7 | 3 | 24 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0002c0007 | 0/0 | 1695 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0002c0011 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0002c0012 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0003c0003 | 1/0 | 1695 | 32 | 26 | 1 | 0 | 0 | 4 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0004c0005 | 0/0 | 1695 | 23 | 8 | 3 | 8 | 2 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0004c0006 | 0/0 | 1695 | 8 | 0 | 0 | 8 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0005c0008 | 0/0 | 1695 | 4 | 0 | 3 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0006c0013 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0006c0014 | 0/0 | 1695 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0007c0010 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0008c0015 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0009c0018 | 0/0 | 1695 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0010c0020 | 0/0 | 1705 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1700): Show |
chr12 | 51276038 | 51329174 | ||
| a0011c0017 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 | ||
| a0012c0016 | 0/0 | 1695 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ATGGC others(1690): Show |
chr12 | 51276038 | 51329174 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2231 | 180 | 34 | 39 | 70 | 8 | 28 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0001c0001t0002 | 0/0 | 2231 | 54 | 10 | 13 | 31 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0001c0001t0003 | 0/0 | 2231 | 11 | 0 | 4 | 0 | 2 | 5 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0001c0001t0004 | 0/0 | 2231 | 3 | 0 | 0 | 3 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0001c0001t0006 | 0/0 | 2231 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0001c0004t0001 | 0/0 | 2231 | 30 | 3 | 4 | 20 | 0 | 3 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0001c0009t0002 | 0/0 | 2231 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0001c0019t0001 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0002c0002t0001 | 0/0 | 2231 | 25 | 3 | 3 | 19 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0002c0002t0002 | 0/0 | 2231 | 9 | 4 | 0 | 5 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0002c0007t0001 | 0/0 | 2231 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0002c0011t0001 | 0/0 | 2231 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0002c0012t0001 | 0/0 | 2231 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0003c0003t0001 | 1/0 | 2231 | 32 | 26 | 1 | 0 | 0 | 4 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0004c0005t0001 | 0/0 | 2231 | 22 | 7 | 3 | 8 | 2 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0004c0005t0005 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0004c0006t0001 | 0/0 | 2231 | 8 | 0 | 0 | 8 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0005c0008t0001 | 0/0 | 2231 | 3 | 0 | 3 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0005c0008t0005 | 0/0 | 2231 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0006c0013t0001 | 0/0 | 2231 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0006c0014t0001 | 0/0 | 2231 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0007c0010t0001 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0008c0015t0001 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0009c0018t0001 | 0/0 | 2231 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0010c0020t0001 | 0/0 | 2241 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2236): Show |
chr12 | 51276038 | 51329174 |
| a0011c0017t0001 | 0/0 | 2231 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| a0012c0016t0001 | 0/0 | 2231 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | ACTTC others(2226): Show |
chr12 | 51276038 | 51329174 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0008 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0007 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0004t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0009t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0009t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0009t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0009t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0001c0019t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0007t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0007t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0007t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0011t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0002c0012t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0003c0003t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0005t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0006t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0006t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0006t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0006t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0004c0006t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0005c0008t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0005c0008t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0005c0008t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0006c0013t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0006c0014t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0007c0010t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0008c0015t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0009c0018t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0010c0020t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0011c0017t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| a0012c0016t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | GBR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00140 | hp2 | a0004 | c0005 | t0001 | g0053 | EUR | GBR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0018 | EUR | FIN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0315 | EUR | FIN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00423 | hp1 | a0001 | c0009 | t0002 | g0170 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00438 | hp1 | a0004 | c0005 | t0001 | g0012 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00597 | hp2 | a0004 | c0005 | t0001 | g0043 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00609 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00621 | hp2 | a0001 | c0004 | t0001 | g0028 | EAS | CHS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00642 | hp1 | a0006 | c0014 | t0001 | g0240 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00738 | hp1 | a0005 | c0008 | t0001 | g0251 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG00741 | hp2 | a0001 | c0004 | t0001 | g0302 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01106 | hp1 | a0004 | c0005 | t0001 | g0045 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01167 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01168 | hp2 | a0004 | c0005 | t0001 | g0013 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0276 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0303 | AMR | PUR | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01256 | hp2 | a0005 | c0008 | t0001 | g0025 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01258 | hp1 | a0005 | c0008 | t0001 | g0025 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01261 | hp2 | a0006 | c0013 | t0001 | g0241 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0264 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01515 | hp2 | a0004 | c0005 | t0001 | g0052 | EUR | IBS | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0126 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0068 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01891 | hp1 | a0001 | c0019 | t0001 | g0254 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0340 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02040 | hp2 | a0004 | c0005 | t0001 | g0044 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0324 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0090 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02056 | hp2 | a0004 | c0005 | t0001 | g0046 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0335 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0343 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02155 | hp1 | a0001 | c0009 | t0002 | g0173 | EAS | CDX | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02257 | hp2 | a0004 | c0005 | t0001 | g0056 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02258 | hp1 | a0003 | c0003 | t0001 | g0006 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0260 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02280 | hp1 | a0004 | c0005 | t0001 | g0013 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0297 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02615 | hp1 | a0003 | c0003 | t0001 | g0348 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02647 | hp1 | a0001 | c0004 | t0001 | g0310 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0092 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0321 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02818 | hp1 | a0004 | c0005 | t0001 | g0014 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02818 | hp2 | a0003 | c0003 | t0001 | g0333 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0070 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0334 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0034 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0034 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0295 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02970 | hp1 | a0007 | c0010 | t0001 | g0065 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02970 | hp2 | a0004 | c0005 | t0001 | g0055 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0069 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0229 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03130 | hp1 | a0004 | c0005 | t0001 | g0060 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0116 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03139 | hp2 | a0008 | c0015 | t0001 | g0154 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03209 | hp1 | a0004 | c0005 | t0005 | g0057 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0271 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03453 | hp2 | a0003 | c0003 | t0001 | g0123 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03486 | hp2 | a0009 | c0018 | t0001 | g0117 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0345 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03491 | hp1 | a0001 | c0004 | t0001 | g0032 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03492 | hp1 | a0001 | c0004 | t0001 | g0032 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0164 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0133 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03704 | hp1 | a0004 | c0005 | t0001 | g0051 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03831 | hp1 | a0004 | c0005 | t0001 | g0054 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0101 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0233 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03927 | hp1 | a0005 | c0008 | t0005 | g0248 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0163 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04184 | hp2 | a0003 | c0003 | t0001 | g0210 | SAS | BEB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0119 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04204 | hp2 | a0010 | c0020 | t0001 | g0346 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | STU | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | YRI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | CHB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | YRI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0336 | AFR | YRI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18942 | hp1 | a0004 | c0006 | t0001 | g0040 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18943 | hp1 | a0004 | c0006 | t0001 | g0049 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18943 | hp2 | a0002 | c0011 | t0001 | g0084 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18946 | hp1 | a0001 | c0009 | t0002 | g0180 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18947 | hp2 | a0004 | c0006 | t0001 | g0047 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18948 | hp1 | a0001 | c0004 | t0001 | g0028 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18951 | hp2 | a0004 | c0006 | t0001 | g0002 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18953 | hp1 | a0002 | c0012 | t0001 | g0077 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18957 | hp2 | a0001 | c0004 | t0001 | g0270 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18961 | hp2 | a0001 | c0004 | t0001 | g0300 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18963 | hp1 | a0001 | c0004 | t0001 | g0030 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18964 | hp1 | a0011 | c0017 | t0001 | g0337 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18966 | hp1 | a0004 | c0006 | t0001 | g0002 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18973 | hp1 | a0001 | c0004 | t0001 | g0253 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18973 | hp2 | a0001 | c0004 | t0001 | g0030 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18978 | hp1 | a0001 | c0009 | t0002 | g0168 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18978 | hp2 | a0002 | c0007 | t0001 | g0072 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18979 | hp2 | a0004 | c0005 | t0001 | g0088 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18980 | hp2 | a0001 | c0004 | t0001 | g0298 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18988 | hp2 | a0002 | c0007 | t0001 | g0062 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18989 | hp2 | a0001 | c0004 | t0001 | g0309 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18990 | hp1 | a0001 | c0004 | t0001 | g0249 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18991 | hp1 | a0004 | c0006 | t0001 | g0002 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18992 | hp1 | a0004 | c0005 | t0001 | g0042 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18992 | hp2 | a0001 | c0004 | t0001 | g0275 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18994 | hp1 | a0012 | c0016 | t0001 | g0156 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18994 | hp2 | a0004 | c0005 | t0001 | g0041 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18995 | hp2 | a0002 | c0007 | t0001 | g0063 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18997 | hp1 | a0001 | c0004 | t0001 | g0278 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19002 | hp1 | a0001 | c0004 | t0001 | g0299 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19011 | hp2 | a0002 | c0007 | t0001 | g0064 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19030 | hp1 | a0004 | c0005 | t0001 | g0061 | AFR | LWK | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19030 | hp2 | a0004 | c0005 | t0001 | g0014 | AFR | LWK | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | LWK | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | LWK | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19054 | hp1 | a0001 | c0004 | t0001 | g0306 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19063 | hp2 | a0004 | c0005 | t0001 | g0012 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19065 | hp2 | a0004 | c0006 | t0001 | g0002 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19066 | hp1 | a0001 | c0004 | t0001 | g0307 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19068 | hp2 | a0001 | c0004 | t0001 | g0325 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19079 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19080 | hp1 | a0001 | c0004 | t0001 | g0277 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19088 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19090 | hp1 | a0004 | c0006 | t0001 | g0048 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | YRI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0294 | AFR | YRI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ASW | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20129 | hp2 | a0003 | c0003 | t0001 | g0341 | AFR | ASW | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | TSI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | TSI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | TSI | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | GIH | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0314 | SAS | GIH | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01123 | hp1 | a0004 | c0005 | t0001 | g0050 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0296 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0228 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0344 | AFR | MSL | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG06807 | hp1 | a0003 | c0003 | t0001 | g0155 | AFR | USA | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | USA | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | USA | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | LWK | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | LWK | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0094 | REF | REF | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0125 | REF | REF | BIN2_chr12_51276038_51329174 | BIN2 | chr12 | 51276038 | 51329174 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51288119 | T | C | 8 | a0001 a0002 a0005 others(5): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
missense_variant | MODERATE | c.1585A>G | p.Asn529Asp | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/13 | 1657/2231 | 1585/1698 | 529/565 | chr12 | 51288119 | |||
| chr12:51291775 | G | A | 1 | a0008 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1331C>T | p.Ser444Leu | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1403/2231 | 1331/1698 | 444/565 | chr12 | 51291775 | |||
| chr12:51291897 | C | A | 1 | a0007 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.1209G>T | p.Lys403Asn | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1281/2231 | 1209/1698 | 403/565 | chr12 | 51291897 | |||
| chr12:51291923 | T | C | 1 | a0005 | 4 | HG00738.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
missense_variant | MODERATE | c.1183A>G | p.Ser395Gly | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1255/2231 | 1183/1698 | 395/565 | chr12 | 51291923 | |||
| chr12:51291932 | G | A | 1 | a0012 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.1174C>T | p.Arg392Cys | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1246/2231 | 1174/1698 | 392/565 | chr12 | 51291932 | |||
| chr12:51299213 | G | A | 1 | a0011 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.592C>T | p.Leu198Phe | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/13 | 664/2231 | 592/1698 | 198/565 | chr12 | 51299213 | |||
| chr12:51299237 | C | T | 1 | a0006 | 2 | HG00642.hp1 HG01261.hp2 |
missense_variant | MODERATE | c.568G>A | p.Glu190Lys | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/13 | 640/2231 | 568/1698 | 190/565 | chr12 | 51299237 | |||
| chr12:51302694 | T | C | 1 | a0009 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.304A>G | p.Ile102Val | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 4/13 | 376/2231 | 304/1698 | 102/565 | chr12 | 51302694 | |||
| chr12:51313842 | C | T | 3 | a0002 a0004 a0007 |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
missense_variant | MODERATE | c.143G>A | p.Ser48Asn | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/13 | 215/2231 | 143/1698 | 48/565 | chr12 | 51313842 | |||
| chr12:51313889 | C | CAATTTCT others(3): Show |
1 | a0010 | 1 | HG04204.hp2 | frameshift_variant | HIGH | c.86_95dupTGCAGAAATT | p.Leu32fs | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/13 | 167/2231 | 95/1698 | 32/565 | chr12 | 51313889 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51291927 | G | A | 1 | a0002c0011 | 1 | NA18943.hp2 | synonymous_variant | LOW | c.1179C>T | p.Thr393Thr | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1251/2231 | 1179/1698 | 393/565 | chr12 | 51291927 | |||
| chr12:51292047 | T | C | 12 | a0001c0001 a0001c0009 a0001c0019 others(9): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
synonymous_variant | LOW | c.1059A>G | p.Glu353Glu | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1131/2231 | 1059/1698 | 353/565 | chr12 | 51292047 | |||
| chr12:51292097 | G | A | 1 | a0001c0009 | 4 | HG00423.hp1 HG02155.hp1 NA18946.hp1 others(1): Show |
synonymous_variant | LOW | c.1009C>T | p.Leu337Leu | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/13 | 1081/2231 | 1009/1698 | 337/565 | chr12 | 51292097 | |||
| chr12:51299628 | T | C | 1 | a0002c0012 | 1 | NA18953.hp1 | synonymous_variant | LOW | c.495A>G | p.Lys165Lys | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 6/13 | 567/2231 | 495/1698 | 165/565 | chr12 | 51299628 | |||
| chr12:51302089 | G | A | 1 | a0004c0006 | 8 | NA18942.hp1 NA18943.hp1 NA18947.hp2 others(5): Show |
synonymous_variant | LOW | c.339C>T | p.Tyr113Tyr | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/13 | 411/2231 | 339/1698 | 113/565 | chr12 | 51302089 | |||
| chr12:51302716 | G | A | 6 | a0002c0002 a0002c0011 a0002c0012 others(3): Show |
68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
synonymous_variant | LOW | c.282C>T | p.Asp94Asp | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 4/13 | 354/2231 | 282/1698 | 94/565 | chr12 | 51302716 | |||
| chr12:51313871 | G | C | 1 | a0001c0019 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.114C>G | p.Thr38Thr | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/13 | 186/2231 | 114/1698 | 38/565 | chr12 | 51313871 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51281082 | C | T | 1 | a0001c0001t0003 | 11 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*417G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 13/13 | 417 | chr12 | 51281082 | ||||||
| chr12:51281167 | T | C | 1 | a0001c0001t0006 | 2 | HG02258.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*332A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 13/13 | 332 | chr12 | 51281167 | ||||||
| chr12:51281177 | T | C | 1 | a0001c0001t0004 | 3 | NA18939.hp2 NA18963.hp2 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*322A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 13/13 | 322 | chr12 | 51281177 | ||||||
| chr12:51281424 | C | T | 3 | a0001c0001t0002 a0001c0009t0002 a0002c0002t0002 |
67 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*75G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 13/13 | 75 | chr12 | 51281424 | ||||||
| chr12:51281462 | C | T | 2 | a0004c0005t0005 a0005c0008t0005 |
2 | HG03209.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*37G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 13/13 | 37 | chr12 | 51281462 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51281660 | A | G | 3 | a0004c0005t0001g0013 a0004c0005t0001g0050 a0004c0005t0001g0053 |
4 | HG00140.hp2 HG01123.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669-132T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51281660 | |||||||
| chr12:51281830 | C | G | 1 | a0001c0001t0002g0216 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1669-302G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51281830 | |||||||
| chr12:51281886 | G | T | 2 | a0001c0001t0001g0339 a0001c0001t0001g0342 |
2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1669-358C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51281886 | |||||||
| chr12:51281959 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1669-431A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51281959 | |||||||
| chr12:51282023 | C | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1669-495G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282023 | |||||||
| chr12:51282119 | T | A | 1 | a0001c0004t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1669-591A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282119 | |||||||
| chr12:51282264 | A | T | 1 | a0002c0012t0001g0077 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1669-736T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282264 | |||||||
| chr12:51282266 | C | CAT | 120 | a0001c0001t0001g0089 a0001c0001t0001g0130 a0001c0001t0001g0209 others(117): Show |
135 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1669-740_1669-739d others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282266 | |||||||
| chr12:51282266 | C | CATAT | 168 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(165): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1669-742_1669-739d others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282266 | |||||||
| chr12:51282467 | A | C | 1 | a0001c0004t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1669-939T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282467 | |||||||
| chr12:51282468 | C | A | 1 | a0001c0004t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1669-940G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282468 | |||||||
| chr12:51282471 | A | C | 1 | a0001c0004t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1669-943T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282471 | |||||||
| chr12:51282674 | C | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0235 a0001c0001t0001g0238 others(3): Show |
8 | HG00738.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1669-1146G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282674 | |||||||
| chr12:51282689 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(268): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1669-1161C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282689 | |||||||
| chr12:51282751 | G | A | 29 | a0003c0003t0001g0119 a0003c0003t0001g0163 a0003c0003t0001g0210 others(26): Show |
35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1669-1223C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282751 | |||||||
| chr12:51282838 | A | G | 1 | a0007c0010t0001g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1669-1310T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282838 | |||||||
| chr12:51282839 | A | G | 20 | a0001c0001t0001g0130 a0001c0001t0006g0260 a0001c0001t0006g0271 others(17): Show |
23 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.1669-1311T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282839 | |||||||
| chr12:51282916 | A | T | 1 | a0001c0004t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1669-1388T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51282916 | |||||||
| chr12:51283130 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1668+1586C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283130 | |||||||
| chr12:51283206 | G | A | 32 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0021 others(29): Show |
41 | HG00323.hp1 HG00558.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1668+1510C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283206 | |||||||
| chr12:51283234 | A | T | 1 | a0001c0004t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1668+1482T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283234 | |||||||
| chr12:51283263 | CA | C | 9 | a0003c0003t0001g0034 a0003c0003t0001g0164 a0003c0003t0001g0297 others(6): Show |
10 | HG02145.hp1 HG02451.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1668+1452delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283263 | |||||||
| chr12:51283263 | CAA | C | 27 | a0003c0003t0001g0119 a0003c0003t0001g0163 a0003c0003t0001g0210 others(24): Show |
33 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1668+1451_1668+145 others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283263 | |||||||
| chr12:51283263 | CAAAA | C | 253 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(250): Show |
288 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.1668+1449_1668+145 others(8): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283263 | |||||||
| chr12:51283263 | CAAAAA | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(31): Show |
42 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1668+1448_1668+145 others(9): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283263 | |||||||
| chr12:51283290 | C | T | 3 | a0001c0001t0001g0227 a0002c0002t0001g0058 a0002c0002t0001g0071 |
3 | HG01109.hp1 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1668+1426G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283290 | |||||||
| chr12:51283304 | A | C | 1 | a0001c0004t0001g0300 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1668+1412T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283304 | |||||||
| chr12:51283323 | C | T | 2 | a0001c0001t0001g0035 a0002c0002t0001g0070 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1668+1393G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283323 | |||||||
| chr12:51283349 | G | A | 18 | a0001c0001t0001g0130 a0002c0002t0001g0003 a0002c0002t0001g0073 others(15): Show |
21 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.1668+1367C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283349 | |||||||
| chr12:51283388 | G | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1668+1328C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283388 | |||||||
| chr12:51283552 | ATCC | A | 6 | a0001c0001t0002g0038 a0001c0001t0002g0218 a0001c0001t0002g0219 others(3): Show |
6 | HG02451.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1668+1161_1668+116 others(7): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283552 | |||||||
| chr12:51283577 | C | T | 1 | a0010c0020t0001g0346 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1668+1139G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283577 | |||||||
| chr12:51283717 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1668+999C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283717 | |||||||
| chr12:51283855 | G | A | 1 | a0010c0020t0001g0346 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1668+861C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283855 | |||||||
| chr12:51283862 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1668+854G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283862 | |||||||
| chr12:51283933 | C | T | 1 | a0003c0003t0001g0344 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1668+783G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283933 | |||||||
| chr12:51283941 | C | T | 2 | a0004c0005t0001g0042 a0007c0010t0001g0065 |
2 | HG02970.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1668+775G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283941 | |||||||
| chr12:51283942 | G | A | 1 | a0002c0002t0001g0073 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1668+774C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283942 | |||||||
| chr12:51283980 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1668+736A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283980 | |||||||
| chr12:51283993 | C | CAA | 32 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0130 others(29): Show |
35 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1668+721_1668+722d others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283993 | |||||||
| chr12:51283993 | C | CAAA | 252 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(249): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1668+720_1668+722d others(5): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283993 | |||||||
| chr12:51283993 | C | CAAAA | 6 | a0001c0001t0001g0021 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
7 | HG01358.hp1 HG02071.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1668+719_1668+722d others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283993 | |||||||
| chr12:51283993 | CA | C | 28 | a0003c0003t0001g0119 a0003c0003t0001g0163 a0003c0003t0001g0210 others(25): Show |
34 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1668+722delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51283993 | |||||||
| chr12:51284007 | A | T | 1 | a0004c0005t0001g0088 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1668+709T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51284007 | |||||||
| chr12:51284248 | C | G | 3 | a0003c0003t0001g0164 a0004c0005t0001g0060 a0004c0005t0001g0061 |
3 | HG03130.hp1 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1668+468G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51284248 | |||||||
| chr12:51284550 | C | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1668+166G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 12/12 | chr12 | 51284550 | |||||||
| chr12:51284809 | C | T | 1 | a0007c0010t0001g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1597-22G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51284809 | |||||||
| chr12:51284820 | G | T | 1 | a0007c0010t0001g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1597-33C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51284820 | |||||||
| chr12:51285112 | T | G | 1 | a0001c0001t0001g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1597-325A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285112 | |||||||
| chr12:51285304 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1597-517C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285304 | |||||||
| chr12:51285463 | T | A | 1 | a0006c0013t0001g0241 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1597-676A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285463 | |||||||
| chr12:51285470 | T | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1597-683A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285470 | |||||||
| chr12:51285484 | A | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0279 a0001c0001t0001g0280 others(8): Show |
13 | HG00642.hp2 HG01261.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1597-697T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285484 | |||||||
| chr12:51285626 | CT | C | 8 | a0001c0001t0002g0191 a0003c0003t0001g0034 a0003c0003t0001g0164 others(5): Show |
9 | HG00558.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1597-840delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285626 | |||||||
| chr12:51285626 | CTT | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(225): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1597-841_1597-840d others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285626 | |||||||
| chr12:51285817 | A | G | 320 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1597-1030T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285817 | |||||||
| chr12:51285820 | A | C | 320 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1597-1033T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285820 | |||||||
| chr12:51285843 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1597-1056G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51285843 | |||||||
| chr12:51286002 | C | T | 5 | a0003c0003t0001g0006 a0003c0003t0001g0126 a0003c0003t0001g0264 others(2): Show |
7 | HG01346.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-1215G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51286002 | |||||||
| chr12:51286026 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1597-1239C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51286026 | |||||||
| chr12:51286080 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1597-1293C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51286080 | |||||||
| chr12:51286202 | G | T | 1 | a0001c0001t0002g0220 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1597-1415C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51286202 | |||||||
| chr12:51286600 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1596+1508C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51286600 | |||||||
| chr12:51286651 | C | T | 29 | a0003c0003t0001g0119 a0003c0003t0001g0163 a0003c0003t0001g0210 others(26): Show |
35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1596+1457G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51286651 | |||||||
| chr12:51287082 | A | G | 18 | a0001c0001t0001g0130 a0002c0002t0001g0003 a0002c0002t0001g0073 others(15): Show |
21 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.1596+1026T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287082 | |||||||
| chr12:51287098 | A | G | 9 | a0001c0001t0001g0089 a0001c0001t0001g0209 a0001c0001t0001g0261 others(6): Show |
9 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+1010T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287098 | |||||||
| chr12:51287123 | C | G | 2 | a0001c0001t0006g0260 a0001c0001t0006g0271 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1596+985G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287123 | |||||||
| chr12:51287236 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1596+872C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287236 | |||||||
| chr12:51287240 | A | T | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1596+868T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287240 | |||||||
| chr12:51287338 | G | GT | 42 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(39): Show |
48 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1596+769dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287338 | |||||||
| chr12:51287338 | G | T | 1 | a0001c0004t0001g0270 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1596+770C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287338 | |||||||
| chr12:51287447 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1596+661G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287447 | |||||||
| chr12:51287572 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1596+536G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287572 | |||||||
| chr12:51287593 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1596+515C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287593 | |||||||
| chr12:51287623 | A | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(324): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1596+485T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287623 | |||||||
| chr12:51287649 | G | GT | 48 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0141 others(45): Show |
54 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1596+458dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287649 | |||||||
| chr12:51287745 | G | A | 29 | a0003c0003t0001g0119 a0003c0003t0001g0163 a0003c0003t0001g0210 others(26): Show |
35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1596+363C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287745 | |||||||
| chr12:51287796 | C | T | 20 | a0001c0001t0001g0130 a0001c0001t0006g0260 a0001c0001t0006g0271 others(17): Show |
23 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.1596+312G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287796 | |||||||
| chr12:51287797 | A | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1596+311T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287797 | |||||||
| chr12:51287837 | G | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1596+271C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287837 | |||||||
| chr12:51287851 | C | A | 2 | a0004c0005t0001g0060 a0004c0005t0001g0061 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1596+257G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51287851 | |||||||
| chr12:51288062 | C | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1596+46G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 11/12 | chr12 | 51288062 | |||||||
| chr12:51288216 | G | C | 1 | a0001c0001t0001g0284 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1516-28C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288216 | |||||||
| chr12:51288352 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1516-164G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288352 | |||||||
| chr12:51288375 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0026 others(47): Show |
59 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1516-187C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288375 | |||||||
| chr12:51288382 | C | A | 1 | a0001c0001t0001g0332 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1516-194G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288382 | |||||||
| chr12:51288609 | C | T | 4 | a0001c0004t0001g0028 a0001c0004t0001g0030 a0001c0004t0001g0270 others(1): Show |
6 | HG00621.hp2 NA18948.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1516-421G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288609 | |||||||
| chr12:51288670 | T | C | 1 | a0004c0006t0001g0047 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1516-482A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288670 | |||||||
| chr12:51288751 | C | CT | 30 | a0003c0003t0001g0119 a0003c0003t0001g0126 a0003c0003t0001g0163 others(27): Show |
36 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.1516-564dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288751 | |||||||
| chr12:51288751 | CT | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(249): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1516-564delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288751 | |||||||
| chr12:51288875 | G | A | 29 | a0003c0003t0001g0119 a0003c0003t0001g0163 a0003c0003t0001g0210 others(26): Show |
35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1516-687C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288875 | |||||||
| chr12:51288905 | T | C | 3 | a0001c0001t0001g0227 a0002c0002t0001g0058 a0002c0002t0001g0071 |
3 | HG01109.hp1 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1516-717A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288905 | |||||||
| chr12:51288941 | G | A | 29 | a0001c0004t0001g0005 a0001c0004t0001g0028 a0001c0004t0001g0030 others(26): Show |
35 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1516-753C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288941 | |||||||
| chr12:51288969 | C | T | 18 | a0001c0001t0001g0130 a0002c0002t0001g0003 a0002c0002t0001g0073 others(15): Show |
21 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.1516-781G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51288969 | |||||||
| chr12:51289040 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1516-852C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289040 | |||||||
| chr12:51289069 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1516-881T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289069 | |||||||
| chr12:51289088 | G | C | 1 | a0001c0001t0002g0201 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1516-900C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289088 | |||||||
| chr12:51289089 | C | G | 1 | a0001c0001t0002g0201 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1516-901G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289089 | |||||||
| chr12:51289111 | G | T | 1 | a0002c0002t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1516-923C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289111 | |||||||
| chr12:51289155 | C | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(316): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1516-967G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289155 | |||||||
| chr12:51289206 | T | A | 320 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1516-1018A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289206 | |||||||
| chr12:51289221 | TA | T | 124 | a0001c0001t0001g0089 a0001c0001t0001g0130 a0001c0001t0001g0209 others(121): Show |
139 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.1516-1034delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289221 | |||||||
| chr12:51289221 | TAAA | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1516-1036_1516-103 others(7): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289221 | |||||||
| chr12:51289304 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1516-1116G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289304 | |||||||
| chr12:51289335 | C | A | 2 | a0001c0001t0006g0260 a0001c0001t0006g0271 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1516-1147G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289335 | |||||||
| chr12:51289723 | A | T | 1 | a0001c0001t0002g0201 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1516-1535T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289723 | |||||||
| chr12:51289922 | C | G | 9 | a0001c0001t0001g0089 a0001c0001t0001g0209 a0001c0001t0001g0261 others(6): Show |
9 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1515+1669G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51289922 | |||||||
| chr12:51290004 | T | A | 18 | a0001c0001t0001g0130 a0002c0002t0001g0003 a0002c0002t0001g0073 others(15): Show |
21 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.1515+1587A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290004 | |||||||
| chr12:51290040 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0131 |
2 | HG01433.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1515+1551G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290040 | |||||||
| chr12:51290191 | C | T | 29 | a0003c0003t0001g0119 a0003c0003t0001g0163 a0003c0003t0001g0210 others(26): Show |
35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1515+1400G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290191 | |||||||
| chr12:51290202 | G | A | 29 | a0001c0004t0001g0005 a0001c0004t0001g0028 a0001c0004t0001g0030 others(26): Show |
35 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1515+1389C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290202 | |||||||
| chr12:51290231 | T | C | 1 | a0001c0001t0002g0178 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1515+1360A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290231 | |||||||
| chr12:51290424 | C | T | 7 | a0003c0003t0001g0034 a0003c0003t0001g0164 a0003c0003t0001g0297 others(4): Show |
8 | HG02145.hp1 HG02451.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1515+1167G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290424 | |||||||
| chr12:51290705 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1515+886C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290705 | |||||||
| chr12:51290777 | C | CA | 18 | a0001c0001t0001g0130 a0002c0002t0001g0003 a0002c0002t0001g0073 others(15): Show |
21 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.1515+813dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290777 | |||||||
| chr12:51290809 | C | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(288): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1515+782G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290809 | |||||||
| chr12:51290849 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(259): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1515+742A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290849 | |||||||
| chr12:51290919 | C | T | 29 | a0003c0003t0001g0119 a0003c0003t0001g0163 a0003c0003t0001g0210 others(26): Show |
35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1515+672G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290919 | |||||||
| chr12:51290927 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1515+664G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290927 | |||||||
| chr12:51290933 | A | AAAAAC | 262 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(259): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1515+653_1515+657d others(7): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51290933 | |||||||
| chr12:51291006 | G | A | 29 | a0003c0003t0001g0119 a0003c0003t0001g0163 a0003c0003t0001g0210 others(26): Show |
35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1515+585C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291006 | |||||||
| chr12:51291040 | T | C | 6 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0263 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+551A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291040 | |||||||
| chr12:51291155 | G | GCAAA | 7 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1515+432_1515+435d others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291155 | |||||||
| chr12:51291172 | C | A | 2 | a0001c0001t0001g0283 a0002c0002t0001g0059 |
2 | HG02027.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1515+419G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291172 | |||||||
| chr12:51291173 | A | C | 7 | a0003c0003t0001g0034 a0003c0003t0001g0164 a0003c0003t0001g0297 others(4): Show |
8 | HG02145.hp1 HG02451.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1515+418T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291173 | |||||||
| chr12:51291176 | A | C | 1 | a0001c0001t0001g0151 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1515+415T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291176 | |||||||
| chr12:51291512 | CAGCCTGG others(1): Show |
C | 3 | a0003c0003t0001g0090 a0003c0003t0001g0116 a0003c0003t0001g0155 |
3 | HG02055.hp2 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1515+71_1515+78del others(8): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 10/12 | chr12 | 51291512 | |||||||
| chr12:51292420 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.762-76A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51292420 | |||||||
| chr12:51292501 | A | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.762-157T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51292501 | |||||||
| chr12:51292590 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.762-246C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51292590 | |||||||
| chr12:51292761 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(240): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.762-417G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51292761 | |||||||
| chr12:51292911 | G | A | 1 | a0001c0001t0001g0332 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.762-567C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51292911 | |||||||
| chr12:51292928 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.762-584A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51292928 | |||||||
| chr12:51293186 | C | G | 2 | a0001c0001t0006g0260 a0001c0001t0006g0271 |
2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.762-842G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293186 | |||||||
| chr12:51293200 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.762-856A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293200 | |||||||
| chr12:51293206 | A | T | 18 | a0001c0001t0001g0130 a0002c0002t0001g0003 a0002c0002t0001g0073 others(15): Show |
21 | HG00408.hp2 HG00609.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.762-862T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293206 | |||||||
| chr12:51293294 | C | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(285): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.762-950G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293294 | |||||||
| chr12:51293357 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0153 |
2 | NA19064.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.762-1013C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293357 | |||||||
| chr12:51293417 | C | T | 1 | a0002c0002t0002g0081 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.762-1073G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293417 | |||||||
| chr12:51293454 | C | T | 1 | a0001c0009t0002g0168 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.762-1110G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293454 | |||||||
| chr12:51293529 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0245 a0001c0001t0001g0250 |
7 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.762-1185C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293529 | |||||||
| chr12:51293546 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(240): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.762-1202G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293546 | |||||||
| chr12:51293599 | A | G | 62 | a0001c0001t0001g0274 a0001c0001t0002g0004 a0001c0001t0002g0022 others(59): Show |
68 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.762-1255T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293599 | |||||||
| chr12:51293604 | G | T | 1 | a0001c0001t0006g0271 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.762-1260C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293604 | |||||||
| chr12:51293655 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.762-1311G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293655 | |||||||
| chr12:51293739 | G | A | 29 | a0001c0004t0001g0005 a0001c0004t0001g0028 a0001c0004t0001g0030 others(26): Show |
35 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.762-1395C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293739 | |||||||
| chr12:51293780 | A | T | 29 | a0003c0003t0001g0119 a0003c0003t0001g0163 a0003c0003t0001g0210 others(26): Show |
35 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.762-1436T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293780 | |||||||
| chr12:51293835 | T | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.762-1491A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293835 | |||||||
| chr12:51293926 | C | A | 1 | a0012c0016t0001g0156 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.762-1582G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293926 | |||||||
| chr12:51293934 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.762-1590C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293934 | |||||||
| chr12:51293957 | C | T | 2 | a0001c0001t0001g0339 a0001c0001t0001g0342 |
2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.762-1613G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51293957 | |||||||
| chr12:51294076 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.761+1720T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294076 | |||||||
| chr12:51294136 | TAAC | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG01361.hp1 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.761+1657_761+1659d others(5): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294136 | |||||||
| chr12:51294196 | T | A | 1 | a0001c0019t0001g0254 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.761+1600A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294196 | |||||||
| chr12:51294207 | A | G | 29 | a0001c0004t0001g0005 a0001c0004t0001g0028 a0001c0004t0001g0030 others(26): Show |
35 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.761+1589T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294207 | |||||||
| chr12:51294264 | T | C | 5 | a0001c0001t0001g0227 a0001c0001t0006g0271 a0002c0002t0001g0058 others(2): Show |
5 | HG01109.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.761+1532A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294264 | |||||||
| chr12:51294296 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.761+1500A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294296 | |||||||
| chr12:51294322 | A | G | 1 | a0001c0001t0003g0099 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.761+1474T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294322 | |||||||
| chr12:51294394 | G | A | 1 | a0001c0001t0006g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.761+1402C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294394 | |||||||
| chr12:51294401 | T | C | 1 | a0007c0010t0001g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.761+1395A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294401 | |||||||
| chr12:51294436 | A | G | 1 | a0003c0003t0001g0155 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.761+1360T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294436 | |||||||
| chr12:51294460 | T | G | 1 | a0001c0004t0001g0296 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.761+1336A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294460 | |||||||
| chr12:51294566 | C | CA | 18 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0107 others(15): Show |
20 | HG00597.hp1 HG01975.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.761+1229dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294566 | |||||||
| chr12:51294566 | CA | C | 72 | a0001c0001t0001g0089 a0001c0001t0001g0140 a0001c0001t0001g0261 others(69): Show |
85 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+1229delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294566 | |||||||
| chr12:51294590 | C | A | 37 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(34): Show |
43 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.761+1206G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294590 | |||||||
| chr12:51294658 | GTTACATT others(5): Show |
G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(231): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.761+1126_761+1137d others(14): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294658 | |||||||
| chr12:51294715 | A | G | 1 | a0008c0015t0001g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.761+1081T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294715 | |||||||
| chr12:51294723 | GCACACAT others(7): Show |
G | 73 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0017 others(70): Show |
84 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.761+1059_761+1072d others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294723 | |||||||
| chr12:51294774 | C | T | 19 | a0001c0001t0002g0190 a0001c0001t0002g0191 a0001c0001t0002g0193 others(16): Show |
19 | HG00558.hp2 HG01978.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.761+1022G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294774 | |||||||
| chr12:51294912 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.761+884C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294912 | |||||||
| chr12:51294974 | C | T | 26 | a0001c0001t0001g0308 a0001c0004t0001g0005 a0001c0004t0001g0028 others(23): Show |
32 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.761+822G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294974 | |||||||
| chr12:51294999 | C | T | 35 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(32): Show |
41 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.761+797G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51294999 | |||||||
| chr12:51295202 | C | T | 1 | a0001c0004t0001g0277 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.761+594G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295202 | |||||||
| chr12:51295234 | C | A | 4 | a0001c0009t0002g0168 a0001c0009t0002g0170 a0001c0009t0002g0173 others(1): Show |
4 | HG00423.hp1 HG02155.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.761+562G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295234 | |||||||
| chr12:51295235 | AT | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(94): Show |
118 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.761+560delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295235 | |||||||
| chr12:51295311 | G | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
87 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.761+485C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295311 | |||||||
| chr12:51295319 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.761+477G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295319 | |||||||
| chr12:51295392 | C | CA | 24 | a0001c0001t0001g0138 a0001c0001t0001g0149 a0001c0001t0001g0286 others(21): Show |
28 | HG00408.hp2 HG00609.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.761+403dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295392 | |||||||
| chr12:51295392 | CAAA | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(40): Show |
52 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.761+401_761+403del others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295392 | |||||||
| chr12:51295392 | CAAAA | C | 108 | a0001c0001t0001g0089 a0001c0001t0001g0134 a0001c0001t0001g0189 others(105): Show |
120 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.761+400_761+403del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295392 | |||||||
| chr12:51295392 | CAAAAAA | C | 26 | a0001c0001t0001g0308 a0001c0004t0001g0005 a0001c0004t0001g0028 others(23): Show |
32 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.761+398_761+403del others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295392 | |||||||
| chr12:51295432 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.761+364C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295432 | |||||||
| chr12:51295500 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.761+296A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295500 | |||||||
| chr12:51295571 | AAAAAAAA others(39): Show |
A | 3 | a0001c0001t0001g0231 a0001c0001t0003g0345 a0001c0001t0004g0109 |
3 | HG03490.hp1 NA18954.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.761+179_761+224del others(46): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295571 | |||||||
| chr12:51295572 | AAAAAAAT others(38): Show |
A | 1 | a0001c0001t0001g0010 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.761+179_761+223del others(45): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295572 | |||||||
| chr12:51295573 | AAAAAATA others(39): Show |
A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0021 others(22): Show |
32 | HG00323.hp1 HG00558.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.761+177_761+222del others(46): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295573 | |||||||
| chr12:51295575 | A | T | 1 | a0003c0003t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.761+221T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295575 | |||||||
| chr12:51295575 | AAAATATA others(17): Show |
A | 1 | a0001c0001t0001g0026 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.761+197_761+220del others(24): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295575 | |||||||
| chr12:51295576 | AAATATAT others(16): Show |
A | 1 | a0002c0002t0001g0039 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.761+197_761+219del others(23): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295576 | |||||||
| chr12:51295576 | AAATATAT others(18): Show |
A | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.761+195_761+219del others(25): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295576 | |||||||
| chr12:51295576 | AAATATAT others(20): Show |
A | 2 | a0001c0001t0006g0260 a0001c0019t0001g0254 |
2 | HG01891.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.761+193_761+219del others(27): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295576 | |||||||
| chr12:51295576 | AAATATAT others(22): Show |
A | 1 | a0003c0003t0001g0340 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.761+191_761+219del others(29): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295576 | |||||||
| chr12:51295576 | AAATATAT others(28): Show |
A | 1 | a0002c0002t0001g0082 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.761+185_761+219del others(35): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295576 | |||||||
| chr12:51295577 | A | T | 2 | a0001c0001t0001g0267 a0003c0003t0001g0163 |
2 | HG02074.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.761+219T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AAT | A | 11 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
11 | HG00099.hp1 HG01928.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.761+217_761+218del others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATAT | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0091 a0001c0001t0001g0093 others(17): Show |
21 | HG00140.hp1 HG00639.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.761+215_761+218del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATAT | A | 16 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0029 others(13): Show |
18 | HG01257.hp1 HG01258.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.761+213_761+218del others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(1): Show |
A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0033 others(8): Show |
13 | HG01975.hp1 HG01993.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.761+211_761+218del others(8): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(3): Show |
A | 10 | a0001c0001t0001g0141 a0001c0001t0001g0268 a0001c0001t0001g0290 others(7): Show |
10 | HG01099.hp2 HG01243.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.761+209_761+218del others(10): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(5): Show |
A | 3 | a0001c0001t0001g0031 a0003c0003t0001g0116 a0003c0003t0001g0155 |
3 | HG00735.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.761+207_761+218del others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(7): Show |
A | 2 | a0001c0001t0001g0019 a0012c0016t0001g0156 |
2 | NA18994.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.761+205_761+218del others(14): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(15): Show |
A | 2 | a0001c0001t0001g0027 a0005c0008t0005g0248 |
3 | HG03490.hp2 HG03492.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.761+197_761+218del others(22): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(17): Show |
A | 11 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0037 others(8): Show |
13 | HG00738.hp1 HG01099.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.761+195_761+218del others(24): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(19): Show |
A | 13 | a0001c0001t0001g0036 a0001c0001t0001g0308 a0001c0004t0001g0005 others(10): Show |
16 | HG00423.hp2 HG00609.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.761+193_761+218del others(26): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(21): Show |
A | 4 | a0001c0004t0001g0276 a0001c0004t0001g0295 a0001c0004t0001g0303 others(1): Show |
4 | HG01192.hp1 HG01243.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.761+191_761+218del others(28): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(23): Show |
A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0338 a0001c0001t0001g0347 |
4 | HG02717.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.761+189_761+218del others(30): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(25): Show |
A | 1 | a0001c0001t0001g0033 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.761+187_761+218del others(32): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(27): Show |
A | 3 | a0001c0001t0002g0183 a0001c0001t0002g0194 a0001c0009t0002g0168 |
3 | HG01981.hp1 NA18978.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.761+185_761+218del others(34): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(29): Show |
A | 25 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0002g0224 others(22): Show |
28 | HG00408.hp2 HG00609.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.761+183_761+218del others(36): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295577 | AATATATA others(37): Show |
A | 27 | a0001c0001t0001g0262 a0003c0003t0001g0210 a0003c0003t0001g0233 others(24): Show |
33 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.761+175_761+218del others(44): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295577 | |||||||
| chr12:51295578 | ATAT | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0152 a0001c0001t0001g0286 |
3 | HG02071.hp2 NA19054.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.761+215_761+217del others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | |||||||
| chr12:51295578 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0315 |
2 | HG00323.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.761+207_761+217del others(11): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | |||||||
| chr12:51295578 | ATATATAT others(6): Show |
A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0209 a0001c0001t0002g0208 |
3 | HG00733.hp2 HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.761+205_761+217del others(13): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | |||||||
| chr12:51295578 | ATATATAT others(10): Show |
A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0146 a0001c0001t0001g0151 |
4 | NA18953.hp2 NA18980.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.761+201_761+217del others(17): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | |||||||
| chr12:51295578 | ATATATAT others(16): Show |
A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG00639.hp1 HG01978.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.761+195_761+217del others(23): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | |||||||
| chr12:51295578 | ATATATAT others(18): Show |
A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0234 others(18): Show |
26 | HG00099.hp2 HG00642.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.761+193_761+217del others(25): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | |||||||
| chr12:51295578 | ATATATAT others(20): Show |
A | 5 | a0001c0004t0001g0028 a0001c0004t0001g0030 a0001c0004t0001g0270 others(2): Show |
7 | HG00621.hp2 HG02451.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.761+191_761+217del others(27): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | |||||||
| chr12:51295578 | ATATATAT others(22): Show |
A | 6 | a0001c0001t0001g0339 a0001c0001t0001g0342 a0001c0004t0001g0005 others(3): Show |
6 | HG01167.hp1 HG02145.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.761+189_761+217del others(29): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | |||||||
| chr12:51295578 | ATATATAT others(28): Show |
A | 63 | a0001c0001t0001g0134 a0001c0001t0001g0189 a0001c0001t0001g0212 others(60): Show |
68 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.761+183_761+217del others(35): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | |||||||
| chr12:51295578 | ATATATAT others(38): Show |
A | 9 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0263 others(6): Show |
9 | HG01346.hp1 HG01884.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.761+173_761+217del others(45): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295578 | |||||||
| chr12:51295579 | T | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
9 | HG01175.hp2 HG01261.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.761+217A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295579 | |||||||
| chr12:51295579 | T | G | 8 | a0002c0002t0001g0058 a0002c0002t0001g0066 a0002c0002t0001g0070 others(5): Show |
9 | HG01109.hp1 HG01167.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.761+217A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295579 | |||||||
| chr12:51295580 | ATATATAT others(28): Show |
A | 8 | a0002c0002t0001g0058 a0002c0002t0001g0066 a0002c0002t0001g0070 others(5): Show |
9 | HG01109.hp1 HG01167.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.761+181_761+215del others(35): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295580 | |||||||
| chr12:51295581 | T | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0136 a0001c0001t0001g0138 others(12): Show |
15 | HG00099.hp1 HG00642.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.761+215A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295581 | |||||||
| chr12:51295583 | T | A | 24 | a0001c0001t0001g0011 a0001c0001t0001g0091 a0001c0001t0001g0095 others(21): Show |
25 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.761+213A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295583 | |||||||
| chr12:51295585 | T | A | 22 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0029 others(19): Show |
26 | HG00140.hp1 HG00639.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.761+211A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295585 | |||||||
| chr12:51295587 | T | A | 21 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0096 others(18): Show |
23 | HG00140.hp1 HG00639.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.761+209A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295587 | |||||||
| chr12:51295589 | T | A | 17 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0128 others(14): Show |
17 | HG01099.hp2 HG01243.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.761+207A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295589 | |||||||
| chr12:51295591 | T | A | 10 | a0001c0001t0001g0031 a0001c0001t0001g0122 a0001c0001t0001g0268 others(7): Show |
10 | HG00323.hp2 HG00735.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.761+205A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295591 | |||||||
| chr12:51295593 | T | A | 6 | a0001c0001t0001g0268 a0001c0001t0001g0315 a0003c0003t0001g0116 others(3): Show |
6 | HG00323.hp2 HG02615.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.761+203A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295593 | |||||||
| chr12:51295595 | T | A | 3 | a0003c0003t0001g0116 a0003c0003t0001g0155 a0003c0003t0001g0229 |
3 | HG03041.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.761+201A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295595 | |||||||
| chr12:51295597 | T | A | 1 | a0001c0001t0001g0009 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.761+199A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295597 | |||||||
| chr12:51295601 | T | A | 2 | a0001c0001t0001g0027 a0005c0008t0005g0248 |
3 | HG03490.hp2 HG03492.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.761+195A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295601 | |||||||
| chr12:51295603 | T | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0242 others(6): Show |
11 | HG00639.hp1 HG00738.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.761+193A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295603 | |||||||
| chr12:51295605 | T | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0234 others(30): Show |
41 | HG00099.hp2 HG00609.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.761+191A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295605 | |||||||
| chr12:51295607 | T | A | 29 | a0001c0001t0001g0234 a0001c0001t0001g0308 a0001c0004t0001g0005 others(26): Show |
34 | HG00609.hp2 HG00621.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.761+189A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295607 | |||||||
| chr12:51295609 | T | A | 34 | a0001c0001t0001g0035 a0001c0001t0001g0308 a0001c0001t0001g0338 others(31): Show |
41 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.761+187A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295609 | |||||||
| chr12:51295611 | T | A | 22 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0308 others(19): Show |
27 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.761+185A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295611 | |||||||
| chr12:51295613 | T | A | 11 | a0001c0001t0001g0033 a0001c0001t0002g0183 a0001c0001t0002g0194 others(8): Show |
11 | HG01167.hp1 HG01192.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.761+183A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295613 | |||||||
| chr12:51295613 | T | G | 1 | a0002c0002t0001g0082 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.761+183A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295613 | |||||||
| chr12:51295614 | A | G | 18 | a0002c0002t0001g0003 a0002c0002t0001g0073 a0002c0002t0001g0074 others(15): Show |
21 | HG00408.hp2 HG00609.hp1 HG03130.hp1 others(18): Show |
intron_variant | MODIFIER | c.761+182T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295614 | |||||||
| chr12:51295615 | T | A | 19 | a0002c0002t0001g0003 a0002c0002t0001g0073 a0002c0002t0001g0074 others(16): Show |
22 | HG00408.hp2 HG00609.hp1 HG03130.hp1 others(19): Show |
intron_variant | MODIFIER | c.761+181A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295615 | |||||||
| chr12:51295615 | T | G | 73 | a0001c0001t0001g0134 a0001c0001t0001g0189 a0001c0001t0001g0212 others(70): Show |
78 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.761+181A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295615 | |||||||
| chr12:51295617 | T | A | 100 | a0001c0001t0001g0134 a0001c0001t0001g0189 a0001c0001t0001g0212 others(97): Show |
109 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.761+179A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295617 | |||||||
| chr12:51295619 | T | A | 100 | a0001c0001t0001g0134 a0001c0001t0001g0189 a0001c0001t0001g0212 others(97): Show |
109 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.761+177A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295619 | |||||||
| chr12:51295620 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.761+176T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295620 | |||||||
| chr12:51295621 | T | A | 100 | a0001c0001t0001g0134 a0001c0001t0001g0189 a0001c0001t0001g0212 others(97): Show |
109 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.761+175A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295621 | |||||||
| chr12:51295623 | T | A | 127 | a0001c0001t0001g0134 a0001c0001t0001g0189 a0001c0001t0001g0212 others(124): Show |
142 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.761+173A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295623 | |||||||
| chr12:51295625 | T | G | 136 | a0001c0001t0001g0089 a0001c0001t0001g0134 a0001c0001t0001g0189 others(133): Show |
151 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.761+171A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295625 | |||||||
| chr12:51295627 | T | A | 136 | a0001c0001t0001g0089 a0001c0001t0001g0134 a0001c0001t0001g0189 others(133): Show |
151 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.761+169A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 9/12 | chr12 | 51295627 | |||||||
| chr12:51295890 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.679-12T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51295890 | |||||||
| chr12:51296177 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.679-299A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296177 | |||||||
| chr12:51296365 | T | A | 1 | a0004c0005t0001g0053 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.679-487A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296365 | |||||||
| chr12:51296390 | G | A | 17 | a0002c0002t0001g0003 a0002c0002t0001g0073 a0002c0002t0001g0074 others(14): Show |
20 | HG00408.hp2 HG00609.hp1 NA18612.hp2 others(17): Show |
intron_variant | MODIFIER | c.679-512C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296390 | |||||||
| chr12:51296496 | C | CA | 12 | a0001c0001t0001g0089 a0001c0001t0001g0257 a0001c0001t0001g0261 others(9): Show |
12 | HG01346.hp1 HG01978.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.678+592dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296496 | |||||||
| chr12:51296496 | CA | C | 26 | a0001c0001t0001g0153 a0001c0001t0001g0308 a0001c0004t0001g0005 others(23): Show |
32 | HG00609.hp2 HG00621.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.678+592delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296496 | |||||||
| chr12:51296510 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.678+579G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296510 | |||||||
| chr12:51296518 | C | A | 2 | a0001c0004t0001g0302 a0001c0004t0001g0310 |
2 | HG00741.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.678+571G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296518 | |||||||
| chr12:51296589 | G | C | 1 | a0001c0001t0001g0322 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.678+500C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296589 | |||||||
| chr12:51296607 | T | C | 9 | a0002c0002t0001g0058 a0002c0002t0001g0066 a0002c0002t0001g0067 others(6): Show |
10 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.678+482A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296607 | |||||||
| chr12:51296729 | A | G | 1 | a0004c0005t0001g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.678+360T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296729 | |||||||
| chr12:51296737 | G | C | 13 | a0002c0002t0001g0003 a0002c0002t0001g0073 a0002c0002t0001g0074 others(10): Show |
16 | HG00408.hp2 HG00609.hp1 NA18612.hp2 others(13): Show |
intron_variant | MODIFIER | c.678+352C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296737 | |||||||
| chr12:51296967 | G | T | 35 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(32): Show |
41 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.678+122C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51296967 | |||||||
| chr12:51297053 | A | C | 1 | a0001c0001t0001g0262 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.678+36T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51297053 | |||||||
| chr12:51297064 | C | T | 1 | a0004c0005t0001g0053 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.678+25G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 8/12 | chr12 | 51297064 | |||||||
| chr12:51297261 | C | A | 1 | a0002c0002t0001g0039 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.603-97G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297261 | |||||||
| chr12:51297343 | C | T | 115 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0029 others(112): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.603-179G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297343 | |||||||
| chr12:51297353 | A | G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0232 |
3 | NA18954.hp2 NA18977.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.603-189T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297353 | |||||||
| chr12:51297364 | C | G | 1 | a0001c0001t0001g0332 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.603-200G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297364 | |||||||
| chr12:51297365 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.603-201T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297365 | |||||||
| chr12:51297379 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.603-215A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297379 | |||||||
| chr12:51297403 | T | TA | 124 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(121): Show |
148 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.603-240dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297403 | |||||||
| chr12:51297423 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.603-259G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297423 | |||||||
| chr12:51297441 | C | T | 3 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0159 |
3 | NA18939.hp2 NA18963.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.603-277G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297441 | |||||||
| chr12:51297629 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(235): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.603-465C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297629 | |||||||
| chr12:51297767 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(194): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.603-603T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297767 | |||||||
| chr12:51297826 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(191): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.603-662G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297826 | |||||||
| chr12:51297838 | G | GT | 190 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(187): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.603-675dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297838 | |||||||
| chr12:51297851 | C | T | 2 | a0001c0001t0002g0203 a0001c0001t0002g0204 |
2 | NA19005.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.603-687G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297851 | |||||||
| chr12:51297879 | C | T | 1 | a0002c0002t0001g0082 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.603-715G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51297879 | |||||||
| chr12:51298000 | C | G | 5 | a0004c0006t0001g0002 a0004c0006t0001g0040 a0004c0006t0001g0047 others(2): Show |
8 | NA18942.hp1 NA18943.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.603-836G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298000 | |||||||
| chr12:51298145 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(188): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.603-981T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298145 | |||||||
| chr12:51298149 | G | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0293 |
2 | NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.603-985C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298149 | |||||||
| chr12:51298168 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(183): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.603-1004A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298168 | |||||||
| chr12:51298197 | C | A | 1 | a0001c0001t0002g0195 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.602+1006G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298197 | |||||||
| chr12:51298320 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.602+883G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298320 | |||||||
| chr12:51298552 | T | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(183): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.602+651A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298552 | |||||||
| chr12:51298556 | T | A | 21 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0073 others(18): Show |
25 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.602+647A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298556 | |||||||
| chr12:51298641 | A | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(55): Show |
70 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.602+562T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298641 | |||||||
| chr12:51298795 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(187): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.602+408T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298795 | |||||||
| chr12:51298894 | C | A | 1 | a0002c0011t0001g0084 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.602+309G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298894 | |||||||
| chr12:51298995 | C | T | 1 | a0001c0004t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.602+208G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51298995 | |||||||
| chr12:51299051 | G | C | 2 | a0004c0005t0001g0060 a0004c0005t0001g0061 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.602+152C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51299051 | |||||||
| chr12:51299092 | G | C | 23 | a0004c0005t0001g0012 a0004c0005t0001g0013 a0004c0005t0001g0014 others(20): Show |
29 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.602+111C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51299092 | |||||||
| chr12:51299093 | GC | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(140): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.602+109delG | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51299093 | |||||||
| chr12:51299094 | C | G | 20 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(17): Show |
21 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.602+109G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 7/12 | chr12 | 51299094 | |||||||
| chr12:51299331 | C | T | 6 | a0002c0002t0001g0066 a0002c0002t0001g0067 a0002c0002t0001g0070 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-43G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 6/12 | chr12 | 51299331 | |||||||
| chr12:51299573 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(187): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.516+34C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 6/12 | chr12 | 51299573 | |||||||
| chr12:51299831 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.409-117G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51299831 | |||||||
| chr12:51299832 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.409-118C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51299832 | |||||||
| chr12:51299848 | G | GT | 141 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(138): Show |
164 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.409-135dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51299848 | |||||||
| chr12:51300118 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(187): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.409-404T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300118 | |||||||
| chr12:51300119 | G | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(187): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.409-405C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300119 | |||||||
| chr12:51300167 | C | T | 1 | a0007c0010t0001g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.409-453G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300167 | |||||||
| chr12:51300249 | T | C | 32 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(29): Show |
37 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.409-535A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300249 | |||||||
| chr12:51300372 | G | A | 91 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(88): Show |
104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.409-658C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300372 | |||||||
| chr12:51300494 | C | T | 91 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(88): Show |
104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.409-780G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300494 | |||||||
| chr12:51300625 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.409-911T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300625 | |||||||
| chr12:51300657 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.409-943C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300657 | |||||||
| chr12:51300737 | C | A | 1 | a0002c0007t0001g0072 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.409-1023G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300737 | |||||||
| chr12:51300811 | T | G | 23 | a0004c0005t0001g0012 a0004c0005t0001g0013 a0004c0005t0001g0014 others(20): Show |
29 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.409-1097A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300811 | |||||||
| chr12:51300959 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0006g0271 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.408+1061C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51300959 | |||||||
| chr12:51301150 | G | A | 1 | a0003c0003t0001g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.408+870C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301150 | |||||||
| chr12:51301183 | A | C | 8 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
8 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+837T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301183 | |||||||
| chr12:51301418 | C | T | 1 | a0007c0010t0001g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.408+602G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301418 | |||||||
| chr12:51301446 | A | G | 1 | a0001c0001t0001g0331 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.408+574T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301446 | |||||||
| chr12:51301500 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0095 a0001c0001t0001g0096 |
4 | HG01070.hp2 HG02735.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+520G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301500 | |||||||
| chr12:51301574 | T | C | 1 | a0001c0004t0001g0299 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.408+446A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301574 | |||||||
| chr12:51301924 | C | T | 53 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(50): Show |
64 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.408+96G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51301924 | |||||||
| chr12:51302007 | GT | G | 23 | a0004c0005t0001g0012 a0004c0005t0001g0013 a0004c0005t0001g0014 others(20): Show |
29 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.408+12delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 5/12 | chr12 | 51302007 | |||||||
| chr12:51302145 | G | T | 6 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(3): Show |
6 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.313-30C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 4/12 | chr12 | 51302145 | |||||||
| chr12:51302163 | A | C | 1 | a0003c0003t0001g0164 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.313-48T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 4/12 | chr12 | 51302163 | |||||||
| chr12:51302316 | C | T | 1 | a0007c0010t0001g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.313-201G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 4/12 | chr12 | 51302316 | |||||||
| chr12:51302638 | C | T | 1 | a0001c0009t0002g0173 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.312+48G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 4/12 | chr12 | 51302638 | |||||||
| chr12:51303302 | G | A | 2 | a0001c0001t0002g0203 a0001c0001t0002g0204 |
2 | NA19005.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.163-161C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51303302 | |||||||
| chr12:51303378 | T | C | 57 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(54): Show |
68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-237A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51303378 | |||||||
| chr12:51303555 | C | T | 1 | a0001c0004t0001g0276 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.163-414G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51303555 | |||||||
| chr12:51303833 | C | A | 1 | a0001c0001t0001g0129 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.163-692G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51303833 | |||||||
| chr12:51303906 | T | C | 1 | a0001c0001t0006g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-765A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51303906 | |||||||
| chr12:51303971 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.163-830C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51303971 | |||||||
| chr12:51304107 | T | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(31): Show |
43 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.163-966A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304107 | |||||||
| chr12:51304159 | C | T | 2 | a0004c0005t0001g0060 a0004c0005t0001g0061 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.163-1018G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304159 | |||||||
| chr12:51304172 | G | A | 6 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(3): Show |
6 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-1031C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304172 | |||||||
| chr12:51304672 | A | C | 148 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(145): Show |
172 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.163-1531T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304672 | |||||||
| chr12:51304714 | A | C | 1 | a0001c0001t0001g0035 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.163-1573T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304714 | |||||||
| chr12:51304835 | T | C | 1 | a0001c0001t0001g0027 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.163-1694A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304835 | |||||||
| chr12:51304982 | T | C | 57 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(54): Show |
68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-1841A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304982 | |||||||
| chr12:51304986 | C | G | 91 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(88): Show |
104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.163-1845G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51304986 | |||||||
| chr12:51305064 | C | T | 6 | a0002c0002t0001g0066 a0002c0002t0001g0067 a0002c0002t0001g0070 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-1923G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305064 | |||||||
| chr12:51305121 | G | A | 1 | a0001c0001t0006g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-1980C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305121 | |||||||
| chr12:51305250 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(31): Show |
43 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.163-2109G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305250 | |||||||
| chr12:51305309 | T | A | 58 | a0001c0001t0002g0038 a0002c0002t0001g0003 a0002c0002t0001g0039 others(55): Show |
69 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.163-2168A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305309 | |||||||
| chr12:51305445 | G | A | 1 | a0003c0003t0001g0335 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-2304C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305445 | |||||||
| chr12:51305523 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.163-2382G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305523 | |||||||
| chr12:51305573 | G | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0002g0224 |
3 | HG02572.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.163-2432C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305573 | |||||||
| chr12:51305596 | C | T | 1 | a0001c0001t0006g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-2455G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305596 | |||||||
| chr12:51305605 | C | G | 1 | a0001c0001t0002g0219 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.163-2464G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305605 | |||||||
| chr12:51305623 | CA | C | 52 | a0001c0001t0001g0122 a0002c0002t0001g0003 a0002c0002t0001g0039 others(49): Show |
63 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.163-2483delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305623 | |||||||
| chr12:51305716 | ATTTAC | A | 2 | a0003c0003t0001g0034 a0003c0003t0001g0336 |
3 | HG02895.hp2 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.163-2580_163-2576d others(7): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305716 | |||||||
| chr12:51305792 | ATT | A | 67 | a0001c0001t0001g0111 a0001c0001t0001g0189 a0001c0001t0001g0209 others(64): Show |
71 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.163-2653_163-2652d others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305792 | |||||||
| chr12:51305826 | C | CT | 62 | a0001c0001t0001g0009 a0001c0001t0001g0089 a0001c0001t0001g0102 others(59): Show |
65 | HG00408.hp1 HG00621.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.163-2686dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305826 | |||||||
| chr12:51305826 | C | CTT | 8 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0121 others(5): Show |
8 | HG00140.hp1 HG00423.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-2687_163-2686d others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305826 | |||||||
| chr12:51305826 | CT | C | 27 | a0001c0001t0002g0205 a0001c0001t0002g0222 a0001c0004t0001g0299 others(24): Show |
31 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.163-2686delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305826 | |||||||
| chr12:51305826 | CTTTT | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(29): Show |
41 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.163-2689_163-2686d others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305826 | |||||||
| chr12:51305829 | T | TC | 3 | a0004c0005t0001g0050 a0004c0005t0001g0056 a0004c0006t0001g0047 |
3 | HG01123.hp1 HG02257.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.163-2689_163-2688i others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305829 | |||||||
| chr12:51305830 | T | C | 32 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0066 others(29): Show |
39 | HG00438.hp1 HG00597.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.163-2689A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305830 | |||||||
| chr12:51305831 | T | C | 22 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0073 others(19): Show |
26 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.163-2690A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305831 | |||||||
| chr12:51305832 | T | C | 1 | a0001c0001t0001g0331 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.163-2691A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305832 | |||||||
| chr12:51305834 | T | C | 1 | a0007c0010t0001g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.163-2693A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305834 | |||||||
| chr12:51305914 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0257 a0001c0001t0001g0258 |
4 | HG00639.hp1 HG01978.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2773T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305914 | |||||||
| chr12:51305998 | G | A | 57 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(54): Show |
68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-2857C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51305998 | |||||||
| chr12:51306035 | A | C | 1 | a0001c0001t0006g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-2894T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306035 | |||||||
| chr12:51306067 | G | A | 57 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(54): Show |
68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-2926C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306067 | |||||||
| chr12:51306134 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(88): Show |
111 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.163-2993A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306134 | |||||||
| chr12:51306238 | T | C | 3 | a0001c0001t0002g0183 a0001c0001t0002g0215 a0001c0001t0002g0217 |
3 | NA18975.hp1 NA19002.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.163-3097A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306238 | |||||||
| chr12:51306266 | C | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(187): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.163-3125G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306266 | |||||||
| chr12:51306305 | T | A | 1 | a0008c0015t0001g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.163-3164A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306305 | |||||||
| chr12:51306356 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(31): Show |
43 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.163-3215C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306356 | |||||||
| chr12:51306403 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(31): Show |
43 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.163-3262C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306403 | |||||||
| chr12:51306519 | C | A | 3 | a0003c0003t0001g0341 a0003c0003t0001g0343 a0003c0003t0001g0344 |
3 | HG02145.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.163-3378G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306519 | |||||||
| chr12:51306519 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.163-3378G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306519 | |||||||
| chr12:51306553 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-3412C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306553 | |||||||
| chr12:51306630 | T | A | 57 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(54): Show |
68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-3489A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306630 | |||||||
| chr12:51306728 | A | T | 57 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(54): Show |
68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-3587T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306728 | |||||||
| chr12:51306737 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-3596G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306737 | |||||||
| chr12:51306789 | A | G | 1 | a0001c0004t0001g0032 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.163-3648T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306789 | |||||||
| chr12:51306793 | T | G | 1 | a0004c0005t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.163-3652A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306793 | |||||||
| chr12:51306843 | T | C | 8 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
8 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-3702A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51306843 | |||||||
| chr12:51307051 | G | A | 4 | a0002c0007t0001g0062 a0002c0007t0001g0063 a0002c0007t0001g0064 others(1): Show |
4 | NA18978.hp2 NA18988.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-3910C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307051 | |||||||
| chr12:51307073 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-3932T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307073 | |||||||
| chr12:51307141 | G | A | 91 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(88): Show |
104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.163-4000C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307141 | |||||||
| chr12:51307223 | C | T | 7 | a0004c0005t0001g0012 a0004c0005t0001g0041 a0004c0005t0001g0042 others(4): Show |
8 | HG00438.hp1 HG00597.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-4082G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307223 | |||||||
| chr12:51307237 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-4096G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307237 | |||||||
| chr12:51307240 | G | A | 2 | a0002c0002t0001g0058 a0002c0002t0001g0071 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.163-4099C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307240 | |||||||
| chr12:51307282 | C | CA | 5 | a0001c0001t0001g0020 a0001c0001t0001g0106 a0001c0001t0001g0137 others(2): Show |
6 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-4142dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307282 | |||||||
| chr12:51307282 | CA | C | 150 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(147): Show |
174 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.163-4142delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307282 | |||||||
| chr12:51307282 | CAA | C | 6 | a0001c0001t0001g0261 a0001c0001t0001g0318 a0001c0004t0001g0300 others(3): Show |
6 | HG01169.hp2 HG02896.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-4143_163-4142d others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307282 | |||||||
| chr12:51307371 | T | A | 91 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(88): Show |
104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.163-4230A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307371 | |||||||
| chr12:51307474 | C | T | 7 | a0001c0001t0001g0098 a0001c0001t0003g0007 a0001c0001t0003g0018 others(4): Show |
10 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-4333G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307474 | |||||||
| chr12:51307491 | C | T | 1 | a0001c0004t0001g0299 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.163-4350G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307491 | |||||||
| chr12:51307507 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(88): Show |
111 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.163-4366T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307507 | |||||||
| chr12:51307710 | C | CA | 26 | a0001c0001t0001g0250 a0001c0001t0002g0207 a0002c0002t0001g0003 others(23): Show |
30 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.163-4570dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307710 | |||||||
| chr12:51307774 | T | C | 2 | a0004c0005t0001g0060 a0004c0005t0001g0061 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.163-4633A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307774 | |||||||
| chr12:51307894 | G | A | 1 | a0003c0003t0001g0006 | 3 | HG02258.hp1 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.163-4753C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307894 | |||||||
| chr12:51307985 | C | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(92): Show |
115 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.163-4844G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51307985 | |||||||
| chr12:51308721 | G | C | 57 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(54): Show |
68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.162+5102C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51308721 | |||||||
| chr12:51309049 | T | C | 4 | a0004c0005t0001g0014 a0004c0005t0001g0055 a0004c0005t0001g0056 others(1): Show |
5 | HG02257.hp2 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+4774A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309049 | |||||||
| chr12:51309130 | C | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(92): Show |
115 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.162+4693G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309130 | |||||||
| chr12:51309360 | T | C | 8 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
8 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+4463A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309360 | |||||||
| chr12:51309554 | AT | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0021 others(27): Show |
38 | HG00323.hp1 HG00558.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.162+4268delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309554 | |||||||
| chr12:51309600 | G | A | 2 | a0002c0002t0001g0058 a0002c0002t0001g0071 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.162+4223C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309600 | |||||||
| chr12:51309662 | T | C | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+4161A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309662 | |||||||
| chr12:51309828 | T | C | 5 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0177 others(2): Show |
5 | NA18949.hp1 NA18959.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+3995A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309828 | |||||||
| chr12:51309977 | G | T | 4 | a0001c0004t0001g0028 a0001c0004t0001g0030 a0001c0004t0001g0270 others(1): Show |
6 | HG00621.hp2 NA18948.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+3846C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51309977 | |||||||
| chr12:51310050 | A | G | 91 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(88): Show |
104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.162+3773T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310050 | |||||||
| chr12:51310174 | T | C | 1 | a0002c0002t0001g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.162+3649A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310174 | |||||||
| chr12:51310187 | G | A | 6 | a0002c0002t0001g0066 a0002c0002t0001g0067 a0002c0002t0001g0070 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.162+3636C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310187 | |||||||
| chr12:51310262 | A | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0142 a0001c0001t0001g0143 others(12): Show |
17 | HG02056.hp1 NA18747.hp2 NA18944.hp2 others(14): Show |
intron_variant | MODIFIER | c.162+3561T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310262 | |||||||
| chr12:51310306 | A | C | 1 | a0001c0001t0002g0230 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.162+3517T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310306 | |||||||
| chr12:51310308 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.162+3515G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310308 | |||||||
| chr12:51310656 | T | A | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+3167A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310656 | |||||||
| chr12:51310788 | T | C | 37 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0066 others(34): Show |
44 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.162+3035A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310788 | |||||||
| chr12:51310806 | A | T | 1 | a0001c0004t0001g0032 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+3017T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51310806 | |||||||
| chr12:51311006 | G | C | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2817C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311006 | |||||||
| chr12:51311041 | G | A | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2782C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311041 | |||||||
| chr12:51311097 | C | CT | 69 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0209 others(66): Show |
73 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.162+2725dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311097 | |||||||
| chr12:51311097 | CT | C | 24 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0073 others(21): Show |
28 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.162+2725delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311097 | |||||||
| chr12:51311196 | C | T | 1 | a0001c0004t0001g0032 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.162+2627G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311196 | |||||||
| chr12:51311302 | G | A | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2521C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311302 | |||||||
| chr12:51311384 | C | CTTATTTA | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2438_162+2439i others(9): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311384 | |||||||
| chr12:51311473 | G | A | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2350C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311473 | |||||||
| chr12:51311567 | G | C | 1 | a0003c0003t0001g0233 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.162+2256C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311567 | |||||||
| chr12:51311570 | G | A | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2253C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311570 | |||||||
| chr12:51311622 | T | C | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2201A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311622 | |||||||
| chr12:51311656 | C | G | 1 | a0003c0003t0001g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.162+2167G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311656 | |||||||
| chr12:51311712 | G | T | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2111C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311712 | |||||||
| chr12:51311730 | A | G | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2093T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311730 | |||||||
| chr12:51311772 | A | ATT | 60 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(57): Show |
71 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.162+2050_162+2051i others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311772 | |||||||
| chr12:51311773 | A | T | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+2050T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311773 | |||||||
| chr12:51311834 | C | T | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+1989G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311834 | |||||||
| chr12:51311899 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(183): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.162+1924T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311899 | |||||||
| chr12:51311983 | G | A | 34 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0035 others(31): Show |
38 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+1840C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51311983 | |||||||
| chr12:51312024 | G | A | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+1799C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312024 | |||||||
| chr12:51312047 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.162+1776A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312047 | |||||||
| chr12:51312051 | C | T | 2 | a0004c0005t0001g0060 a0004c0005t0001g0061 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.162+1772G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312051 | |||||||
| chr12:51312196 | T | G | 3 | a0001c0001t0001g0209 a0001c0001t0002g0208 a0003c0003t0001g0164 |
3 | HG02109.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.162+1627A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312196 | |||||||
| chr12:51312411 | A | T | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.162+1412T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312411 | |||||||
| chr12:51312520 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.162+1303G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312520 | |||||||
| chr12:51312683 | A | G | 1 | a0004c0005t0001g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.162+1140T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312683 | |||||||
| chr12:51312764 | A | T | 22 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0073 others(19): Show |
26 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.162+1059T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51312764 | |||||||
| chr12:51313184 | G | GAGGA | 20 | a0001c0001t0001g0089 a0001c0001t0001g0121 a0001c0001t0001g0128 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.162+635_162+638dup others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313184 | |||||||
| chr12:51313184 | G | GAGGAAGG others(1): Show |
104 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0033 others(101): Show |
114 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.162+631_162+638dup others(8): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313184 | |||||||
| chr12:51313184 | G | GAGGAAGG others(5): Show |
36 | a0001c0001t0001g0029 a0001c0001t0001g0237 a0001c0001t0001g0279 others(33): Show |
42 | HG00609.hp2 HG00621.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.162+627_162+638dup others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313184 | |||||||
| chr12:51313184 | G | GAGGAAGG others(9): Show |
13 | a0001c0001t0001g0225 a0001c0001t0001g0272 a0001c0001t0001g0304 others(10): Show |
14 | HG01168.hp1 HG01169.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.162+623_162+638dup others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313184 | |||||||
| chr12:51313184 | GAGGA | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0130 |
3 | HG02083.hp1 NA18968.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.162+635_162+638del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313184 | |||||||
| chr12:51313184 | GAGGAAGG others(5): Show |
G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0157 others(1): Show |
7 | HG02155.hp2 NA18939.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.162+627_162+638del others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313184 | |||||||
| chr12:51313215 | G | GAAGGAAG others(9): Show |
1 | a0001c0004t0001g0309 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.162+607_162+608ins others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313215 | |||||||
| chr12:51313216 | A | AAGGAAGG others(9): Show |
5 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0252 others(2): Show |
6 | HG00423.hp2 HG00738.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+606_162+607ins others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313216 | |||||||
| chr12:51313216 | A | AAGGAAGG others(5): Show |
25 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0026 others(22): Show |
32 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.162+606_162+607ins others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313216 | |||||||
| chr12:51313216 | A | AAGGAAGG others(5): Show |
1 | a0001c0001t0001g0238 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162+606_162+607ins others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313216 | |||||||
| chr12:51313220 | A | AAGGAAGG others(17): Show |
2 | a0002c0002t0001g0039 a0002c0002t0002g0086 |
2 | HG02523.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.162+602_162+603ins others(24): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313220 | |||||||
| chr12:51313220 | A | AAGGAAGG others(13): Show |
15 | a0002c0002t0001g0003 a0002c0002t0001g0073 a0002c0002t0001g0074 others(12): Show |
19 | HG00408.hp2 HG00609.hp1 NA18612.hp2 others(16): Show |
intron_variant | MODIFIER | c.162+602_162+603ins others(20): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313220 | |||||||
| chr12:51313220 | A | AAGGAAGG others(9): Show |
3 | a0002c0002t0001g0075 a0002c0011t0001g0084 a0007c0010t0001g0065 |
3 | HG02970.hp1 NA18943.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.162+602_162+603ins others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313220 | |||||||
| chr12:51313220 | A | AAGGAAGG others(13): Show |
1 | a0002c0002t0002g0081 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.162+602_162+603ins others(20): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313220 | |||||||
| chr12:51313220 | A | AAGGAAGG others(5): Show |
3 | a0001c0004t0001g0276 a0002c0002t0002g0085 a0003c0003t0001g0294 |
3 | HG01192.hp1 NA19083.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.162+602_162+603ins others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313220 | |||||||
| chr12:51313220 | A | C | 1 | a0001c0001t0003g0101 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.162+603T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313220 | |||||||
| chr12:51313224 | C | A | 31 | a0002c0002t0001g0058 a0002c0002t0001g0071 a0002c0007t0001g0062 others(28): Show |
37 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.162+599G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313224 | |||||||
| chr12:51313228 | A | AAGGAAGG others(5): Show |
1 | a0004c0005t0001g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.162+594_162+595ins others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313228 | |||||||
| chr12:51313228 | A | AAGGC | 5 | a0001c0004t0001g0253 a0004c0005t0001g0014 a0004c0005t0001g0055 others(2): Show |
6 | HG02257.hp2 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+591_162+594dup others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313228 | |||||||
| chr12:51313228 | A | AAGGCAGG others(1): Show |
3 | a0001c0001t0001g0023 a0001c0001t0001g0257 a0001c0001t0006g0260 |
4 | HG01433.hp2 HG01496.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+587_162+594dup others(8): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313228 | |||||||
| chr12:51313228 | A | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0026 others(66): Show |
85 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.162+595T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313228 | |||||||
| chr12:51313307 | C | T | 61 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(58): Show |
68 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.162+516G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313307 | |||||||
| chr12:51313346 | C | CT | 91 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(88): Show |
104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.162+476dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313346 | |||||||
| chr12:51313593 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0107 others(2): Show |
8 | HG02155.hp2 NA18939.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.162+230C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313593 | |||||||
| chr12:51313593 | G | C | 1 | a0001c0001t0001g0035 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.162+230C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313593 | |||||||
| chr12:51313698 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.162+125T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 2/12 | chr12 | 51313698 | |||||||
| chr12:51314017 | C | CTTAT | 25 | a0001c0001t0001g0019 a0001c0001t0001g0091 a0001c0001t0001g0093 others(22): Show |
26 | HG00639.hp2 HG01070.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.82-118_82-115dupAT others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314017 | |||||||
| chr12:51314017 | CTTAT | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(168): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.82-118_82-115delAT others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314017 | |||||||
| chr12:51314017 | CTTATTTA others(1): Show |
C | 102 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0102 others(99): Show |
123 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.82-122_82-115delAT others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314017 | |||||||
| chr12:51314017 | CTTATTTA others(5): Show |
C | 6 | a0001c0001t0001g0108 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
6 | NA18939.hp2 NA18948.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-126_82-115delAT others(10): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314017 | |||||||
| chr12:51314017 | CTTATTTA others(9): Show |
C | 1 | a0001c0001t0001g0326 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.82-130_82-115delAT others(14): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314017 | |||||||
| chr12:51314021 | T | C | 1 | a0011c0017t0001g0337 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.82-118A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314021 | |||||||
| chr12:51314070 | C | T | 22 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0073 others(19): Show |
26 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.82-167G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314070 | |||||||
| chr12:51314080 | C | G | 1 | a0008c0015t0001g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.82-177G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314080 | |||||||
| chr12:51314129 | C | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0002g0224 |
3 | HG02572.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.82-226G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314129 | |||||||
| chr12:51314132 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(93): Show |
116 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.82-229A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314132 | |||||||
| chr12:51314199 | C | T | 6 | a0002c0002t0001g0066 a0002c0002t0001g0067 a0002c0002t0001g0070 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-296G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314199 | |||||||
| chr12:51314204 | C | T | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-301G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314204 | |||||||
| chr12:51314237 | G | A | 27 | a0002c0007t0001g0062 a0002c0007t0001g0063 a0002c0007t0001g0064 others(24): Show |
33 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.82-334C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314237 | |||||||
| chr12:51314413 | C | T | 1 | a0002c0002t0002g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.82-510G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314413 | |||||||
| chr12:51314435 | A | G | 52 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0209 others(49): Show |
56 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.82-532T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314435 | |||||||
| chr12:51314521 | T | C | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-618A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314521 | |||||||
| chr12:51314540 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(184): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.82-637A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314540 | |||||||
| chr12:51314542 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.82-639C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314542 | |||||||
| chr12:51314597 | C | T | 1 | a0001c0001t0001g0332 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-694G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314597 | |||||||
| chr12:51314714 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.82-811C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314714 | |||||||
| chr12:51314753 | C | T | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-850G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314753 | |||||||
| chr12:51314780 | C | T | 37 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0066 others(34): Show |
44 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.82-877G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314780 | |||||||
| chr12:51314799 | C | CA | 38 | a0001c0001t0002g0179 a0002c0002t0001g0058 a0002c0002t0001g0059 others(35): Show |
45 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.82-897dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314799 | |||||||
| chr12:51314799 | C | CAA | 20 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0073 others(17): Show |
24 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-898_82-897dupTT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314799 | |||||||
| chr12:51314821 | T | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(94): Show |
117 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.82-918A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314821 | |||||||
| chr12:51314930 | A | G | 12 | a0002c0007t0001g0062 a0002c0007t0001g0063 a0002c0007t0001g0064 others(9): Show |
13 | HG00438.hp1 HG00597.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.82-1027T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314930 | |||||||
| chr12:51314962 | T | TC | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-1060dupG | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51314962 | |||||||
| chr12:51315099 | T | C | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-1196A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315099 | |||||||
| chr12:51315174 | A | ATT | 19 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0074 others(16): Show |
23 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.82-1273_82-1272dup others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315174 | |||||||
| chr12:51315174 | A | T | 48 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0001g0189 others(45): Show |
51 | HG00558.hp2 HG00597.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-1271T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315174 | |||||||
| chr12:51315174 | AT | A | 40 | a0001c0001t0001g0255 a0001c0009t0002g0180 a0002c0002t0001g0058 others(37): Show |
47 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.82-1272delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315174 | |||||||
| chr12:51315177 | T | A | 28 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0089 others(25): Show |
30 | HG00639.hp2 HG01175.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.82-1274A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315177 | |||||||
| chr12:51315178 | T | A | 11 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0070 others(8): Show |
12 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-1275A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315178 | |||||||
| chr12:51315180 | T | A | 8 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
8 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-1277A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315180 | |||||||
| chr12:51315207 | T | C | 1 | a0001c0004t0001g0310 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.82-1304A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315207 | |||||||
| chr12:51315297 | T | G | 6 | a0002c0002t0001g0066 a0002c0002t0001g0067 a0002c0002t0001g0070 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-1394A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315297 | |||||||
| chr12:51315319 | C | A | 6 | a0002c0002t0001g0066 a0002c0002t0001g0067 a0002c0002t0001g0070 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-1416G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315319 | |||||||
| chr12:51315328 | G | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG01081.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.82-1425C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315328 | |||||||
| chr12:51315378 | T | C | 90 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(87): Show |
103 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.82-1475A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315378 | |||||||
| chr12:51315395 | A | C | 1 | a0004c0006t0001g0040 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.82-1492T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315395 | |||||||
| chr12:51315423 | C | T | 2 | a0004c0005t0001g0060 a0004c0005t0001g0061 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.82-1520G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315423 | |||||||
| chr12:51315498 | T | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(32): Show |
44 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.82-1595A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315498 | |||||||
| chr12:51315538 | G | A | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-1635C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315538 | |||||||
| chr12:51315633 | G | T | 1 | a0001c0001t0006g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.82-1730C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315633 | |||||||
| chr12:51315661 | G | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG00140.hp1 HG01081.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.82-1758C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315661 | |||||||
| chr12:51315667 | C | T | 11 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(8): Show |
12 | HG02145.hp1 HG02559.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-1764G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315667 | |||||||
| chr12:51315706 | T | A | 62 | a0001c0001t0002g0038 a0002c0002t0001g0003 a0002c0002t0001g0039 others(59): Show |
73 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.82-1803A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315706 | |||||||
| chr12:51315871 | C | A | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-1968G>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51315871 | |||||||
| chr12:51316048 | ACCAT | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0257 a0001c0001t0001g0258 |
4 | HG00639.hp1 HG01978.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-2149_82-2146del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316048 | |||||||
| chr12:51316218 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.82-2315G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316218 | |||||||
| chr12:51316290 | C | T | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-2387G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316290 | |||||||
| chr12:51316328 | C | CA | 141 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0089 others(138): Show |
159 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.82-2426dupT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316328 | |||||||
| chr12:51316328 | C | CAA | 83 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(80): Show |
95 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.82-2427_82-2426dup others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316328 | |||||||
| chr12:51316328 | C | CAAA | 17 | a0001c0001t0001g0033 a0001c0001t0001g0162 a0001c0001t0001g0267 others(14): Show |
18 | HG00099.hp1 HG00642.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.82-2428_82-2426dup others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316328 | |||||||
| chr12:51316328 | CA | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(31): Show |
43 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.82-2426delT | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316328 | |||||||
| chr12:51316422 | T | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(259): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.82-2519A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316422 | |||||||
| chr12:51316482 | G | A | 2 | a0004c0005t0001g0060 a0004c0005t0001g0061 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.82-2579C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316482 | |||||||
| chr12:51316561 | A | C | 62 | a0001c0001t0002g0038 a0002c0002t0001g0003 a0002c0002t0001g0039 others(59): Show |
73 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.82-2658T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316561 | |||||||
| chr12:51316695 | C | T | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-2792G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51316695 | |||||||
| chr12:51317267 | A | G | 53 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0209 others(50): Show |
57 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.82-3364T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317267 | |||||||
| chr12:51317316 | T | G | 1 | a0002c0011t0001g0084 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.82-3413A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317316 | |||||||
| chr12:51317341 | G | C | 3 | a0001c0001t0002g0230 a0003c0003t0001g0228 a0003c0003t0001g0229 |
3 | HG02559.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.82-3438C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317341 | |||||||
| chr12:51317352 | G | C | 1 | a0003c0003t0001g0155 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.82-3449C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317352 | |||||||
| chr12:51317365 | T | C | 1 | a0002c0002t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82-3462A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317365 | |||||||
| chr12:51317559 | C | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0021 others(26): Show |
37 | HG00323.hp1 HG00558.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.82-3656G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317559 | |||||||
| chr12:51317613 | C | T | 1 | a0001c0001t0006g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.82-3710G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317613 | |||||||
| chr12:51317676 | T | C | 1 | a0012c0016t0001g0156 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.82-3773A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317676 | |||||||
| chr12:51317711 | G | A | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.82-3808C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317711 | |||||||
| chr12:51317779 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.82-3876C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317779 | |||||||
| chr12:51317839 | T | G | 1 | a0001c0001t0001g0037 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.82-3936A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317839 | |||||||
| chr12:51317950 | C | T | 61 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0058 others(58): Show |
72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-4047G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51317950 | |||||||
| chr12:51318121 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.82-4218G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318121 | |||||||
| chr12:51318233 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.82-4330C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318233 | |||||||
| chr12:51318262 | C | CT | 91 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(88): Show |
104 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.82-4360dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318262 | |||||||
| chr12:51318390 | T | C | 1 | a0002c0002t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82-4487A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318390 | |||||||
| chr12:51318465 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0157 others(1): Show |
7 | HG02155.hp2 NA18939.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-4562A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318465 | |||||||
| chr12:51318468 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.82-4565C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318468 | |||||||
| chr12:51318479 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.82-4576G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318479 | |||||||
| chr12:51318535 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(101): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.82-4632A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318535 | |||||||
| chr12:51318559 | G | A | 1 | a0001c0001t0001g0332 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-4656C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318559 | |||||||
| chr12:51318774 | A | T | 1 | a0001c0001t0002g0097 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.82-4871T>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318774 | |||||||
| chr12:51318817 | G | A | 1 | a0001c0001t0004g0159 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.82-4914C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318817 | |||||||
| chr12:51318896 | TTTTGGTT others(12): Show |
T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0095 a0001c0001t0001g0096 |
4 | HG01070.hp2 HG02735.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-5012_82-4994del others(19): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318896 | |||||||
| chr12:51318957 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.82-5054G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51318957 | |||||||
| chr12:51319130 | T | A | 1 | a0001c0001t0001g0267 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.81+4892A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319130 | |||||||
| chr12:51319267 | C | T | 22 | a0002c0007t0001g0062 a0002c0007t0001g0063 a0002c0007t0001g0072 others(19): Show |
27 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.81+4755G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319267 | |||||||
| chr12:51319272 | G | C | 1 | a0001c0001t0003g0160 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.81+4750C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319272 | |||||||
| chr12:51319399 | T | C | 47 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(44): Show |
54 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.81+4623A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319399 | |||||||
| chr12:51319421 | G | A | 2 | a0004c0005t0001g0060 a0004c0005t0001g0061 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.81+4601C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319421 | |||||||
| chr12:51319646 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(192): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.81+4376T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319646 | |||||||
| chr12:51319802 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.81+4220G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319802 | |||||||
| chr12:51319921 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.81+4101C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319921 | |||||||
| chr12:51319953 | T | C | 4 | a0002c0007t0001g0062 a0002c0007t0001g0063 a0002c0007t0001g0064 others(1): Show |
4 | NA18978.hp2 NA18988.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+4069A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319953 | |||||||
| chr12:51319955 | C | CTCTCCTT others(7): Show |
4 | a0002c0007t0001g0062 a0002c0007t0001g0063 a0002c0007t0001g0064 others(1): Show |
4 | NA18978.hp2 NA18988.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+4066_81+4067ins others(14): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319955 | |||||||
| chr12:51319955 | C | CTCTCTCC others(9): Show |
187 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(184): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.81+4066_81+4067ins others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319955 | |||||||
| chr12:51319982 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(188): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.81+4040G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319982 | |||||||
| chr12:51319985 | C | G | 90 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(87): Show |
103 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.81+4037G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51319985 | |||||||
| chr12:51320162 | G | A | 7 | a0002c0002t0001g0066 a0002c0002t0001g0067 a0002c0002t0001g0070 others(4): Show |
8 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+3860C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320162 | |||||||
| chr12:51320631 | ATTC | A | 81 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(78): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.81+3388_81+3390del others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320631 | |||||||
| chr12:51320631 | ATTCT | A | 5 | a0003c0003t0001g0034 a0003c0003t0001g0333 a0003c0003t0001g0334 others(2): Show |
6 | HG02145.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+3387_81+3390del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320631 | |||||||
| chr12:51320634 | C | CT | 7 | a0001c0001t0001g0091 a0001c0001t0001g0134 a0001c0001t0001g0138 others(4): Show |
7 | HG00323.hp1 NA18955.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+3387dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320634 | |||||||
| chr12:51320634 | CT | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0111 others(8): Show |
11 | HG01070.hp1 HG01993.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.81+3387delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320634 | |||||||
| chr12:51320634 | CTTT | C | 42 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(39): Show |
48 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.81+3385_81+3387del others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320634 | |||||||
| chr12:51320634 | CTTTT | C | 22 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0073 others(19): Show |
27 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.81+3384_81+3387del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320634 | |||||||
| chr12:51320636 | T | A | 2 | a0001c0001t0001g0273 a0001c0004t0001g0314 |
2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.81+3386A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320636 | |||||||
| chr12:51320637 | T | A | 81 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(78): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.81+3385A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320637 | |||||||
| chr12:51320638 | T | A | 5 | a0003c0003t0001g0034 a0003c0003t0001g0333 a0003c0003t0001g0334 others(2): Show |
6 | HG02145.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+3384A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320638 | |||||||
| chr12:51320639 | T | A | 1 | a0001c0004t0001g0314 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.81+3383A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320639 | |||||||
| chr12:51320640 | T | A | 31 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0035 others(28): Show |
35 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.81+3382A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320640 | |||||||
| chr12:51320641 | T | A | 5 | a0003c0003t0001g0034 a0003c0003t0001g0333 a0003c0003t0001g0334 others(2): Show |
6 | HG02145.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+3381A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320641 | |||||||
| chr12:51320644 | T | A | 1 | a0003c0003t0001g0336 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.81+3378A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320644 | |||||||
| chr12:51320786 | T | A | 156 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(153): Show |
180 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.81+3236A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320786 | |||||||
| chr12:51320801 | AGAG | A | 6 | a0002c0002t0001g0066 a0002c0002t0001g0067 a0002c0002t0001g0070 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+3218_81+3220del others(3): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320801 | |||||||
| chr12:51320934 | A | AAC | 7 | a0002c0002t0001g0066 a0002c0002t0001g0067 a0002c0002t0001g0070 others(4): Show |
8 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACAC | 8 | a0001c0001t0001g0262 a0001c0001t0001g0265 a0001c0001t0001g0339 others(5): Show |
8 | HG01346.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACAC | 6 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0006g0260 others(3): Show |
6 | HG00408.hp2 HG01192.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(6): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(1): Show |
17 | a0001c0001t0001g0263 a0001c0001t0001g0316 a0002c0002t0001g0003 others(14): Show |
21 | HG00609.hp1 HG02145.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(8): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(3): Show |
4 | a0001c0001t0001g0027 a0002c0002t0001g0076 a0002c0002t0002g0081 others(1): Show |
5 | HG00438.hp2 HG02055.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(10): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(5): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0026 others(9): Show |
12 | HG01515.hp1 HG01978.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(12): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(7): Show |
21 | a0001c0001t0001g0011 a0001c0001t0001g0162 a0001c0001t0001g0234 others(18): Show |
21 | HG00099.hp1 HG01071.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(14): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(19): Show |
1 | a0001c0001t0001g0273 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+3087_81+3088ins others(26): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(9): Show |
21 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0236 others(18): Show |
21 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(16): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(11): Show |
22 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(19): Show |
23 | HG00099.hp2 HG00642.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(18): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(13): Show |
16 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0033 others(13): Show |
18 | HG01071.hp1 HG01106.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(20): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(15): Show |
11 | a0001c0001t0001g0245 a0001c0001t0001g0315 a0001c0004t0001g0005 others(8): Show |
12 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(22): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(17): Show |
13 | a0001c0001t0001g0256 a0001c0001t0001g0286 a0001c0004t0001g0005 others(10): Show |
13 | HG00609.hp2 HG01891.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(24): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(19): Show |
11 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0267 others(8): Show |
11 | HG00733.hp2 HG01346.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(26): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(21): Show |
15 | a0001c0001t0001g0029 a0001c0001t0001g0320 a0001c0001t0001g0332 others(12): Show |
15 | HG00741.hp2 HG02886.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(28): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(23): Show |
4 | a0001c0001t0001g0289 a0001c0001t0001g0311 a0001c0001t0001g0317 others(1): Show |
4 | HG01496.hp2 NA18951.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(30): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(25): Show |
1 | a0001c0001t0001g0281 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.81+3087_81+3088ins others(32): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(27): Show |
3 | a0001c0001t0001g0292 a0001c0001t0001g0301 a0001c0004t0001g0032 |
4 | HG03491.hp1 HG03492.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(34): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | AACACACA others(29): Show |
1 | a0001c0001t0001g0285 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.81+3087_81+3088ins others(36): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | ACACACAC others(6): Show |
1 | a0005c0008t0001g0251 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.81+3087_81+3088ins others(13): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | ACACACAC others(12): Show |
1 | a0006c0014t0001g0240 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.81+3087_81+3088ins others(19): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | ACACACAC others(14): Show |
3 | a0001c0001t0001g0001 a0001c0004t0001g0277 a0004c0005t0001g0056 |
3 | HG01070.hp1 HG02257.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(21): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | ACACACAC others(18): Show |
1 | a0003c0003t0001g0335 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.81+3087_81+3088ins others(25): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | ACACACAC others(24): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0347 |
2 | HG00735.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.81+3087_81+3088ins others(31): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320934 | A | C | 1 | a0002c0002t0001g0073 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.81+3088T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320934 | |||||||
| chr12:51320936 | A | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(187): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.81+3086T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320936 | |||||||
| chr12:51320941 | A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0235 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.81+3080_81+3081ins others(13): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320941 | |||||||
| chr12:51320954 | A | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(188): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.81+3068T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320954 | |||||||
| chr12:51320971 | T | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(188): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.81+3051A>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51320971 | |||||||
| chr12:51321099 | T | G | 1 | a0002c0007t0001g0072 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.81+2923A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321099 | |||||||
| chr12:51321135 | TGAGA | T | 155 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(152): Show |
179 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.81+2883_81+2886del others(4): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321135 | |||||||
| chr12:51321194 | G | A | 18 | a0002c0002t0001g0003 a0002c0002t0001g0039 a0002c0002t0001g0073 others(15): Show |
22 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.81+2828C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321194 | |||||||
| chr12:51321370 | G | A | 1 | a0001c0001t0002g0182 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.81+2652C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321370 | |||||||
| chr12:51321565 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(187): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.81+2457C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321565 | |||||||
| chr12:51321616 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.81+2406G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321616 | |||||||
| chr12:51321823 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.81+2199T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321823 | |||||||
| chr12:51321861 | T | C | 1 | a0001c0001t0006g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81+2161A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321861 | |||||||
| chr12:51321876 | CTT | C | 3 | a0002c0002t0002g0016 a0002c0002t0002g0085 a0002c0002t0002g0086 |
4 | NA18982.hp1 NA18995.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+2144_81+2145del others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321876 | |||||||
| chr12:51321897 | T | G | 155 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(152): Show |
179 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.81+2125A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321897 | |||||||
| chr12:51321930 | G | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(187): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.81+2092C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51321930 | |||||||
| chr12:51322012 | G | T | 1 | a0001c0001t0002g0183 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.81+2010C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322012 | |||||||
| chr12:51322146 | ACT | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(33): Show |
45 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.81+1874_81+1875del others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322146 | |||||||
| chr12:51322159 | T | C | 1 | a0002c0002t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.81+1863A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322159 | |||||||
| chr12:51322178 | A | C | 1 | a0001c0001t0001g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.81+1844T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322178 | |||||||
| chr12:51322390 | A | C | 6 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0001g0262 others(3): Show |
6 | HG01346.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+1632T>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322390 | |||||||
| chr12:51322440 | A | AGTGTG | 1 | a0003c0003t0001g0006 | 3 | HG02258.hp1 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.81+1577_81+1581dup others(5): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322440 | |||||||
| chr12:51322550 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.81+1472G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322550 | |||||||
| chr12:51322607 | G | GT | 21 | a0001c0001t0001g0091 a0001c0001t0001g0165 a0001c0001t0002g0004 others(18): Show |
24 | HG00423.hp1 HG00621.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.81+1414dupA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322607 | |||||||
| chr12:51322607 | G | T | 1 | a0001c0001t0003g0092 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.81+1415C>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322607 | |||||||
| chr12:51322607 | GT | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(188): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.81+1414delA | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322607 | |||||||
| chr12:51322614 | T | G | 155 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(152): Show |
179 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.81+1408A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322614 | |||||||
| chr12:51322627 | C | T | 1 | a0002c0002t0001g0039 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.81+1395G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322627 | |||||||
| chr12:51322700 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.81+1322G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322700 | |||||||
| chr12:51322797 | CTT | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(188): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.81+1223_81+1224del others(2): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322797 | |||||||
| chr12:51322809 | C | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0347 |
2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.81+1213G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322809 | |||||||
| chr12:51322920 | C | T | 1 | a0003c0003t0001g0164 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.81+1102G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322920 | |||||||
| chr12:51322982 | G | A | 154 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0031 others(151): Show |
178 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.81+1040C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51322982 | |||||||
| chr12:51323297 | G | A | 1 | a0004c0005t0001g0088 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.81+725C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323297 | |||||||
| chr12:51323310 | C | T | 1 | a0003c0003t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.81+712G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323310 | |||||||
| chr12:51323400 | T | TCTGAACA others(33): Show |
9 | a0001c0001t0001g0035 a0001c0001t0001g0338 a0001c0001t0001g0339 others(6): Show |
10 | HG01891.hp2 HG02145.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+582_81+621dupGA others(38): Show |
BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323400 | |||||||
| chr12:51323462 | G | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0023 others(260): Show |
300 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.81+560C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323462 | |||||||
| chr12:51323463 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.81+559T>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323463 | |||||||
| chr12:51323487 | T | C | 1 | a0001c0001t0003g0345 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.81+535A>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323487 | |||||||
| chr12:51323490 | G | C | 1 | a0010c0020t0001g0346 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.81+532C>G | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323490 | |||||||
| chr12:51323525 | C | G | 58 | a0001c0001t0002g0038 a0002c0002t0001g0003 a0002c0002t0001g0039 others(55): Show |
69 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.81+497G>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323525 | |||||||
| chr12:51323641 | T | G | 1 | a0001c0001t0001g0347 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.81+381A>C | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323641 | |||||||
| chr12:51323754 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG00423.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.81+268G>A | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323754 | |||||||
| chr12:51323817 | G | A | 1 | a0003c0003t0001g0348 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81+205C>T | BIN2 | ENSG00000110934.13 | transcript | ENST00000615107.6 | protein_coding | 1/12 | chr12 | 51323817 |